Anti-inflammatory steroid 2&#39;-acetamido-2&#39;-deoxy-glucoside compounds



United States Patent 3,325,474 ANTI-INFLAMMATORY STEROID 2'-ACETAMIDO- 2'-DEOXY-GLUCOSIDE COMPOUNDS Lewis H. Sarett, Princeton, Robert G. Strachan, Summit, and Ralph F. Hirschmann, Scotch Plains, N.J., assignors to Merck & Co., Inc., Rahway, N.J., a corporation of New Jersey No Drawing. Filed Oct. 6, 1964, Ser. No. 402,015 12 Claims. (Cl. 260--210.5)

pregnane series. In other aspects, the invention is con cerned with processes by which the novel compounds may be prepared and with pharmaceutical compositions containing them. The compounds of this invention, especially ring A unsaturated steroid derivatives including the preferred 21-hydoxy derivatives, possess the anti-inflammatory activity characteristic of cortisone, hydrocortisome, and their A -derivatives, prednisone and prednisolone. The steroid derivatives are remarkably free from the ulcerogenic action, adrenal atrophy, thymus involution 1 and body weight loss side-elfects which have resulted from prolonged administration of the aforementioned antiinflammatory steroids. The compounds of the invention are especially interesting because of their delayed absorption with resulting prolonged effect on oral administration.

Novel 21-yl compounds which are the preferred compounds within the scope of this invention may be represented by the formulas:

I II wherein ZCH- is a radical of a ring A unsaturated l1,17-bis-oxygenated-20-keto-Zl-hydroxy steroid of the pregnane series formed by removal of the hydrogen of the hydroxyl group. Compounds represented by Formula I are glucoside derivatives and those represented by Formula II are galactoside derivatives. Novel 16-yl compounds may be similarly represented by replacing Z CH with a 16-hydroxy steroid radical in which the hydrogen atom of the hydroxyl group is replaced with the glucoside or galactoside moiety.

These preferred compounds may be prepared by reacting the selected 2l-free alcohol with a 2-lower alkanoyl amido compound such as 2-acetamido-3,4,6-tri-O-acyl-1- chloro2-deoxy-a-D-glucose or with the corresponding galactose. The most convenient triacyl compounds are the O-triacetates and the reaction will be described using these compounds which Will be referred to hereinafter as 1-chloro-N-acetylglucosamine triacetate and l-chloro-N- acetylgalactosamine triacetate. The products formed by up the O-triacetate derivative 12 and/or 3,325,474 Patented June 13, 1 967 2 this reaction are 3',4',6'-triacetates, namely steroid-2l-yltri O acetyl-[iD-2'-acetamido-2-deoxy gluoosides and galactosides. The O-acetyl groups are then removed by hydrolysis.

The reactions as applied to the preparation of glucosides may be represented as follows:

CH OY In theforegoing formulas- Z-CH O- has thesamemeaning as above. The 16- hydoxy derivatives are sin'iilarlyprepared from 21-acyl compound, as are derivativesfof other hydroxylated anti inflammatory compounds.

The O-triacetate derivatives are conveniently prepared The hydrolysis reaction, which is preferably carried out in an inert atmosphere, is conveniently conducted by taking in alower alcohol such as methanol containing a metal alcoholate such as sodium. methoxide and maintaining the mixture at room lated by any convenient method. For example, the mixture can be adjusted to neutrality with. a lower acid followed by the addition of water and cooling. The product which separates on cooling is usually crystalline and is recovered by filtration.

In accordance with tho e procedures, there are obtained N-alkanoyl; for example N-acetamido-2-deoxy-glucosides and galactosides of the following compounds which include the preferred Ring A unsaturated 11,l7-bis-oxygenated-ZI-hydroxy-20-keto-pregnanes of the anti-inflammatory pregnane series: salicylic acid, hydroxybutazolidine, cortisone, hydrocortisone, and the A -derivatives thereof, prednisone and prednisolone; A and/or 16-hydroxy derivatives (including acetonides) of any of the foregoing; derivatives of any of these compounds having fluoro, chloro or bromo substituents attached to the 6, 9, 16-carbon atoms, and/or methyl substituents I HC-NHO O CH: 8) i temperav ture for from ten minutes to an hour. The product is isoalkanoic, I

attached to the 2, 6, 12, 15 and/ or 16 carbon atoms; and the like. Of particular interest are the derivatives of 16- methyl cortisone and hydrocortisone especially the 6,16- dirnethyl compounds and their A -derivatives and [3,2-c] pyrazolo derivatives thereof.

The new compounds of this invention are stable and possess anti-inflammatory activity characteristic of cortisone but exhibit greatly reduced undesirable side effects. They are normally administered in a daily maintenance dosage range comparable with that of the parent compound. For example, with the cortison and hydrocortisone derivatives the daily dosage is about 25 to 75 mg., for prednisolone it is about 2.5 to 10mg. and for dexamethasone 0.25 to mg. Because of their selective anti-inflammatory action (substantially unaccompanied by undesired side effects) they may, in acute cases be administered in substantially higher dosages without attendant risk of side effects; and, in milder conditions, may often be administered in substantially lower dosages in view of their pronounced anti-inflammatory action directly at the sight of the inflammation.

The compounds of this invention may be administered alone or associated with a pharmaceutically acceptable carrier the choice of which will depend upon the chosen route of administration, and standard pharmaceutical practice. For oral administration, the compounds may be administered in the form of tablets containing excipients such as starch or milk sugar. Aqueous solutions such as elixirs which may be sweetened by flavoring may also be employed. For parenteral use, isotonic mixtures in pryogen-free water may be employed.

1-chloro-N-acetylglucosamine triacetate used as a starting material in the preparation of the compounds of this invention in accordance with the process described above is prepared by the following procedure.

A solution of 23 g. of clean sodium in 1000 ml. of methanol is used in equal portions as described below: 21.5 g. of glusoamine hydrochloride and a 100 ml. aliquot of the above solution is swirled in a 250 ml. Erlenmeyer flask for exactly 70 seconds. The sodium chloride which separates is removed by filtration under pressure through a sintered glass funnel with a 2 1. round bottom flask. This operation is repeated nine more times and the total filter cake washed with 100 ml. of methanol. The total filtrate in the flask is treated under nitrogen with 153 g. of acetic anhydride and warmed for a short time. The solution is then stirred for approximately fifteen hours during which time the N-acetylglucosamine precipitates in approximately 70% yield. It is recovered by filtration, washed extensively with methanol and dried to constant weight, M.P. 202204.

This product is converted to the 1-chloro-O-triacetate derivative by the following procedure.

A suspension of 25 g. of N-acetylglucosamine and 70 ml. of acetyl chloride is stirred under nitrogen for ten minutes..At this point, 1 ml. of acetic acid saturated with HCl gas (at 0) is added and after minutes the mixture starts to gently reflux. At the end of two hours all of the material is in a yellow brown solution. The mixture is then stirred for approximately 15 hours, 500 ml. of chloroform is added, the mixture poured into 1 kg. of ice and stirred for three minutes. (The balance of this procedure should be carried out as rapidly as possible to insure maximum yields.) The mixture is separated and the chloroform layer added rapidly to an ice cold saturated. sodium bicarbonate solution with vigorous stir-ring. The slightly alkaline mixture is again separated and the chloroform layer washed once with water, dried over anhydrous sodium sulfate, filtered and the filtrate evaporated to dryness in vacuo at about 35 C. The residue is taken up in ethyl acetate at 55-66", filtered, seeded and the product allowed to crystallize overnight in the cold. The yield is 26.8 g. The product is protected from light and stored in-a tightly stoppered container in the refrigerator. i l V 4 1-chloro-N-acetylgalactosamine triacetate is prepared as described hereinabove but starting with galactosamine hydrochloride instead of glucosamine hydrochloride.

The following examples are given by way of illustration only and are not intended as limitations of this invention, many apparent variations of which are possible without departing from the spirit and scope thereof.

EXAMPLE I 11,17-Dihydroxy-3,20-di0ne-1,4-pr6gnaa'iene-21-yl-D-2- acetamido -Z-de0xy-gluc0pyranoside A total of 4.5 g. of 1l,l7,2l-trihydroxy-1,4-pregnadiene-3,20-dione is taken up in 25 ml. of dry dimethylformamide containing 17.6 g. of mercuric cyanide and the mixture diluted with 25 ml. of dry xylene. A solution of 13.0 g. of 1-chloro-N-acetylglucosamine triacetate in ml. of 1:1 dimethylformarnide-xylene is added drop- Wise over a period of three hours while stirring the mixture under nitrogen at an oil bath temperature of 130-135 C. The mixture turns quite dark during the addition. It is maintained at 130135 C. for an additional one and three quarter hours, cooled, diluted with 500 ml. of chloroform and washed four times with 500 ml. portions of water.

The aqueous layers are successively back-extracted with chloroform, the combined organic layers dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo. The residue is taken up in ethylene chloride and the solvent again removed in vacuo. The residue is then flushed twice with toluene and pumped (oil pump) at about 50 for several hours and then at room temperature overnight. The residue is taken up in chloroform and chromatographed on acid washed alumina (only about 10.5 parts alumina/part of solution) keeping the height to diameter ratio of alumina in the column at about 8:1. The column is eluted with methanol-chloroform mixtures containing successively larger proportions of methanol up to 95:5. The product, 11B,17a-dihydroxy- 3,20-dione-1,4-pregnadiene-2l-yl-tri-O-acetyl t3 D 2- acetamido-2'-deoxy-glucopyranoside is recovered from the middle fractions. Each fraction is taken to dryness. The first 2-3 fractions consist of a mobile oil. A small amount of methanol is added to subsequent fractions and those which crystallize on scratching are redissolved in chloroform, combined, filtered, taken to dryness and crystallized from ethanol.

A .solution of 1.055 g. of the product thus prepared in ml. of spectral grade methanol is treated with an equivalent quantity of freshly prepared sodium methoxide and kept at room temperature in a nitrogen atmosphere for ten minutes. The pH of the solution is adjusted to neutrality with acetic acid and the mixture filtered. About 6.5 ml. of water is added and the solution centrifuged. The desired product starts to precipitate in about ten minutes and the mixture is kept cold overnight. The desired product is recovered by filtration.

The procedure of the foregoing example is utilized to prepare 21-yl-B-D 2-acetamido-2'-deoxy glucopy-ranosides and galactopyranosides of the following compounds. In each instance the intermediate O-triacetate is prepared. The list is given to avoid unnecessary repetition of experimental details.

16a-methyl-1 1fi,17oc,2 l-trihydroxy-l ,4-pregnadiene-3 ,20-

' dione,

16 3-methyl-1lfl,17a,21-trihydroxy-1,4-pregnadiene-3,Z0-

dione,

9u-fluoro-16wmethyl-1 lfi,17a,21-trihydroxy-1,4-pregnadiene-3 ,20-dione,

6ot-methyl-11p,170:,2l-trihydroxy1,4-pregnadiene-3,20-

dione,

6a-fluoro-11fi,17a,2l-trihydroxy-1,4-pregnadiene-3,20-

dione,

60:, 1 6a-dimethyl-1 1,8,17ot,2l-trihydroxy-1,4-pregnadiene- 3 ,ZO-dione,

6,16a-dimethyl11B,17a,2ltrihydroxy-1,4,6-

pregnatriene-3,ZO-dione,

9u-fluoro-1 1,8,16a,17,2l-tetrahydroxy-l,4-pregnadiene- 3 ,ZO-dione,

9a-fluoro-6,l6ot-dimethyl-11B,17a,21trihydroxy-1,4,6-

pregnatriene-3 ,ZO-dione,

17e,21-dihydroxy-1-allopregnene-3,l1,20-triene,

1 l-B,17u,21-trihydroxy-2-phenyl-[3,2-c]-pyrazolo4- pregnene-ZO-one,

16oc-methyl-l 1B,17a,2l-trihydroxy-[3 ,2-c] -pyrazolo-4- pregnene-20-one,

17a,21-dihydroxy-4-pregnene-3,11,20-triene,

6,16a-dimethyl*11/3,17ot,2l-trihydroxy-[3,2-c]-Pyrazolo- 4,6-pregnadiene-20-one,

6,16a-dimethy1-11,8,17a,21-trihydroxy-2phenyl-[3,2-c]- pyrazolo-4,6-.pregnadiene-20-one,

6,16a-dimethyl-1 1fi,17a,21-trihydroxy-4,6-pregnadiene- 3 ,20-dione,

EXAMPLE II 911 fluoro 1]fi,]7oc,21 trihydroxy 3,20 dz'one 1,4- pregnadz'iene 16cc yl ,8 D 2' aceiamz'do 2' deoxy glucoside A total of 9 g. of 9u-fluoro-21-acetoxy-115,17ot-dihydroxy-1,4-pregnadiene-3,20-dione is taken up in 50 ml. of dimethylformamide containing 36 g. of mercuric cyanide and the mixture diluted with 50 ml. of dry xylene. A solution of 1-chloro-N-acetylglucosamine triacetate in 200 ml. of 1:1 dimethylformamide-xylene is added dropwise over a period of three hours while stirring the mixture under nitrogen at an oil bath temperature of 130- 135 C. The mixture turns dark during the addition. It is maintained at 130-135 C. for an additional two hours, cooled, diluted with one liter of chloroform and washed four times with 500 ml. portions of water. The aqueous layers are successively back-extracted with chloroform, the combined organic layers dried over anhydrous magnesium sulfate, filtered and the filtrate evaporated in vacuo. The residue is taken up in ethylene chloride and the solvent again removed in vacuo. The residue is twice flushed with toluene (oil pump) at about 50 for several hours and then at room temperature overnight. The product, 9ot-fluoro-21-acetoxy1l5,17wdihydroxy-3,20-dione- 1,4-pregnadiene 16a yl tri O acetyl B D 2'- acetamido 2' deoxy glucoside is separated on acid washed alumina using mixtures of chloroform and methanol.

This product is hydrolyzed in accordance with the procedure of Example I to obtain the desired product.

The procedure of the foregoing example is utilized to prepare 16a yl ,8-D-2-acetamido-2-deoxy-glucopyranosides and galactosides of the following compounds. In each instance the intermediate O-triacetate is prepared. The list is given to avoid unnecessary repetition of experimental details.

9a-fiuoro2-methyl-115,16a,17a,21-tetrahydroxy-1,4-

pregn adiene-3,20-dion e,

6 6a,9a-difluoro-2-methyl-1 1,8,16a,17a,21-tetrahydroxy-4- pregnene-3,20-dione, 6a,9ot-difiuoro-2amethyl-1 1B,16a,17a,21-tetrahydroXy- 1,4-pregnadiene-3,20 dione.

EXAMPLE III Ortho-carbomethoxyphenyl-fl-D-Z -aCetamid0-2'- deoxy-glucoside To a mixture of 62.3 g. of anhydrous potassium carbonate, 34.7 ml. of methyl salicylate and 1380 ml. of acetone is added 57 g. of 1-chloro-N-acetylglucosamine triacetate. The mixture is stirred at room temperature for 21 hours and filtered. The solvent is removed at low pressure and the residue triturated with ether to crystallize O carbomethoxyphenyl tri O acetyl p D 2- acetamido-2'-glucoside which is converted to orthocarbomethoxyphenyl-/3-D-2-acetamido-2'-deoxy glucoside by hydrolysis with sodium methoxide in accordance with the procedures of the foregoing examples.

To a suspension of 30.1 g. of the above-prepared compound in one liter of Water is added 87 ml. of 1 N sodium hydroxide solution. The mixture is stirred for three hours and sufficient Dry Ice (about 5 g.) added to clear the solution. When the Dry Ice disappears, the mixture is freeze-dried to yield the desired product as the sodium salt. It may be purified by recrystallization from ethanol or methanol-isopropanol mixtures.

The sodium salt is converted to the acid by acidifying a cold, concentrated solution of the salt, filtering quickly and washing with a small amount of cold water.

Each of the compounds in this example is generally useful as an anti-inflammatory compound in the same manner as aspirin. They are especially useful since they behave similarly to enteric-coated capsules. On oral administration, there is a delay before significant amounts are absorbed. Moreover, the release of the total active ingredient is prolonged over an extended period of time.

Galactosides of these compounds which are similarly useful are prepared in the same manner.

EXAMPLE IV H ydroxybuiazo lidine-B-D-Z'-aceta nido-2'- deoxy-glucoside A mixture containing 500 mg. of hydroxybutazolidine and 1.6 mM. of sodium hydroxide and an equivalent amount of 1-chloro-N-acetylglucosamine triacetate in 500 ml. of acetone is stirred under nitrogen at room temperature for three hours. At the end of this time the solvent and a small amount of Water is removed by distillation at low pressure. The residue is Washed with water and taken up in methylene chloride. The insoluble portion is removed by filtration and the filtrate distilled at low pressure to leave the desired product as a residue.

The O-acetyl groups are removed using methanol and sodium methoxide in accordance with the procedure of Example I.

The corresponding galactosaminide is similarly prepared.

The compounds prepared in accordance with this example are useful in the same manner as those prepared in Example III.

Various changes and modifications may be made in A solution of 10.22 g. of methyl iodide in 50 ml. of ether is added to 1.73 g. of magnesium in 50 ml. of ether. To the resulting ethereal solution of methyl magnesium iodide, maintained under a nitrogen atmosphere, is added 0.045 g. of anhydrous cuprous chloride. To this mixture is added, over a period of about one hour, during which period the reaction mixture is stirred vigorously and maintained at approximately room temperature, a solution of about 5.6 g. of 3a-acetoxy-16-pregnene-11,20-dione in 175 ml. of ether. A white granular solid separates during this addition. The resulting mixture is heated under gentle reflux for two hours after which the reaction mixture is cooled, and 125 ml. of saturated, aqueous ammonium chloride solution is added followed by 200 ml. of ether. The layers are separated, and the ethereal layer is washed with three 50 ml. portions of water. The washed ethereal layer is dried, and the solvent evaporated in vacuo to give a brown viscous oil. The latter material is heated for 15 minutes at 6070 C. with a mixture of 25 ml. acetic anhydride and 25 ml. pyridine and the acetylated product is purified by chromatography on acid-washed alumina followed by crystallization from petroleum ether to give approximately 1.5 g. of substantially pure 3a-acetoxy- 16u-methyl-pregnane-1 1,20-dione.

To a solution of 0.8 g. of 3u-acetoxy-16a-methyl-pregnane-ll,20-dione in 40 ml. of methanol is added 1.5 ml. of concentrated aqueous hydrochloric acid and the resulting solution is stirred overnight at about 25 C. The reaction solution is evaporated in vacuo at 25 C. to a small volume, and the concentrated solution is poured into 50 ml. of ice water. The white solid which precipitates is recovered by filtration, washed with water and recrystallized from ethyl acetate to give 3a-hydroxy-l6tx-rnethyl-preg nane-l 1 ,20-dione.

A solution of 22 g. of 3a-acetoxy-16u-methyl-pregnane- 11,20-dione and l g. of p-toluene-sulfonic acid in 250 ml. of acetic anhydride is heated at reflux under nitrogen for a period of approximately 3 days. Two grams of potassium acetate (anhydrous) is added, and the volatile solvents are separated by distillation in vacuo. The residual material is extracted with benzene, and the benzene extract is filtered to remove insoluble material. The benzene extracts are evaporated to a volume of 100' ml. and petroleum ether is added to the cloud point. The resulting solution is adsorbed on 660 g. of acid-washed alumina; the alumina adsorbate is then washed with 2 liters of petroleum ether. The adsorbate is then eluted with 85:15 petroleum ether-ether mixture, and the first four liters of eluate is collected, and evaporated to dryness in vacuo to give a mixture of enol acetates containing 3a,20-diacetoxy-l6a-methyl-l7(20)-pregnene-ll-one. This mixture of enolates, weighing approximately 14 g., is dissolved in 50 ml. of benzene and treated with an excess of perbenzoic acid over a 16-hour period. The reaction mixture is shaken with dilute aqueous potassium hydroxide solution until the benzene layer is free of per-benzoic acid; the benzene layer is then washed with water until neutral, dried, and the solvent evaporated in vacuo to give a crystalline material, 17a,20-epoxy-3a,20-diacetoxy-160tmethyl-pregnane-ll-one. The latter material is dissolved, without purification, in 200 ml. of methanol, 120 ml. of water and g. of potassium bicarbonate, and the resulting solution is heated at reflux under nitrogen for a period of 16 hours. The methanol is evaporated from the hydrolysis solution in vacuo, and the residual oil is extracted from the resulting aqueous solution with chloro; form. The chloroform extract is washed with water to neutrality, dried, and the chloroform is evaporated under reduced pressure. The residual oil is triturated with ether, and the crystalline material thus formed is recrystallized from ethyl acetate-petroleum ether to give 3a,17 x-dihydroxy-l 6a-methyl-pregnane-l 1 ,20-di one.

To a solution of 7.0 g. of 3a,Not-dihydroxy-16a-methylpregnane-11,20-dione in 50 ml. of chloroform is added dropwise with stirring a solution containing 3.36 g. of

bromine in 24.2 ml. of chloroform over a period of about 60 minutes. he reaction mixture is dissolved in 200 ml. of ethyl acetate, and the resulting solution washed with water until neutral, dried, and the solvents evaporated therefrom in vacuo. The residual crude material is dissolved in a minimum quantity of ethyl acetate, the resulting solution is diluted with ether, and the mixture is stirred until crystals form. The crystalline product is recovered by filtration and washed, by stirring, with 50:50 ether-petroleum ether mixture to give about 5 g. of 21 bromo-3a,l7a-dihydroxy-16ot-methyl-pregnane-11, 20-dione.

This 5 g. of 21 bromo 304,170: -di'hydroxy 160a methyl pregnane 11,20 dione is mixed with 5.0 g. of anhydrous potassium acetate, 4.0 g. of sodium iodide and 0.03 ml. of glacial acetic acid, and ml. of acetone is added to the resulting mixture. This mixture is then heated at reflux, with stirring, for a period of about 16 hours, and the reaction mixture is cooled, filtered, and the insoluble material is washed with acetone. The filtered solution is evaporated in vacuo thereby removing the solvents, and the residual material is slurried with water. and the aqueous mixture extracted with ethyl acetate. The ethyl acetate extract is washed with water to neutrality, dried, and the solvent is evaporated in vacuo to give an oil. This oil is crystallized from ether, and recrystallized from ethyl acetate ether to give 304,170c,21 trihydroxy 16a methyl pregnane 11,20 dione 21-acetate.

Solution of 400 mg. of 3u,l7a,2l trihydroxy 16amethyl pregnane 11,20 dione 21 acetate in 4 ml. of pyridine is added to the complex formed by the addition of 400 mg. of chromium trioxide to 4 ml. of pyridine. The mixture is swirled until thoroughly mixed, and then allowed to stand at room temperature overnight. The reaction mixture is poured into water, and the aqueous mixture is extracted with ether, and then twice with ethyl acetate. The combined ether and ethyl acetate extracts are washed with dilute aqueous sulfuric acid at about 0 C., and then with water until neutral. The organic solvent layer is then dried, the solvents are evaporated therefrom in vacuo, and the residual crystalline material is purified by crystallization from ethyl acetate to give 17oc,21 dihydroxy 16a methyl pregnane 3, 11,20-trione 2l-acetate.

To 100 mg. of 17a,21 dihydroxy a methylpregnane 3,11,20 trione 21 acetate dissolved in 2 ml. of chloroform and 2.25 ml. of glacial acetic acid, at a temperature of -55 C., is added two drops of a 0.001 N solution of dry H Br in glacial acetic acid. To about 0.38 ml. of 0.001 N HBr in glacial acetic acid, at -55 C., is added 0.43 ml. of a solution containing 40 mg. of bromine in chloroform, and the resulting solution is added, over about a lO-minute period, to the solution of the steroid, while maintaining the reaction mixture at about -55 C. The reaction mixture is allowed to stand at 55 C. for about one-half hour; a solution containing 250 mg. of sodium acetate in 3 ml. of water is added, and the resulting mixture is stirred for about 5 minutes. Five milliliters of water are then added, and the aqueous mixture is extracted with ethyl acetate. The ethyl acetate extract is washed with aqueous sodium bicarbonate solution to neutrality, then with water, dried, and the solvent is evaporated in vacuo. The residual material is dissolved in 2 ml. of acetone, and to the solution is added 25 mg. of sodium bromide and 1 ml. of water. The resulting mixture is heated under reflux for a period of about 5 hours, the reaction mixture is cooled, and the acetone is evaporated in vacuo. The residual material is extracted into ether, the ether extract is washed with water, dried, and the solvent is evaporated to a volume of about 1 m1.; petroleum ether is added to this solution, and the crystalline material which separates is recovered and dried to give approximately 90 mg. of 4-bromo-17a,21-dihydroxy-16u-methylpregnane-3,1 1,20-trione Zl-acetate.

A mixture of 48 mg. of semicarbazide, 48 mg. of 4- bromo 1711,21 dihydroxy 16a methyl pregnane 3, 11,20-trione 21-acetate and 0.6 ml. of ethanol is heated under reflux in contact with a nitrogen atmosphere for a period of about three days, and the reaction solution is evaporated to a small volume, diluted with water and the crystalline material recovered and purified by recrystallization from equeous methanol to give 3,20-bissemicarbazido-17a, 21 dihydroxy 160a methyl 4- pregnene-3,l1,20-trione ZI-acetate. Fifty milligrams of 3, 20 bis semicarbazido 1711,21 dihydroxy lfiu-methyl- 4 pregnene 3,11,20 trione 21-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1.1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is recrystallized from ethyl acetate to give 3,20 bis semicarbazido 17oc,2l dihydroxyl6ot methyl 4-pregnene-3,11,20-trione.

A mixture of 60 mg. of 3,20 bis semicarbazido-17a, 21 dihydroxy 16a methyl 4 pregnene-3,11,20- trione, 0.2 ml. of dimethylformamide, 0.6 ml. of chloroform, and 1.5 ml. of 1.0 N aqueous hydrochloric acid is heated under reflux for a period of about three hours. The resulting two-phase system is cooled to a temperature of approximately C., and the layers are separated. The aqueous layer I and the chloroform extracts are combined with the original chloroform dimethylformamide solution. The combined organic layer is washed with an aqueous solution of sodium bicarbonate, and the chloroform and dimethylformamide in the combined organic layer is replaced with ethyl acetate by evaporation in vacuo. Petroleum ether is added and the resulting solution is subjected to a partition chromatogram using aqueous methanol as the stationary phase and benzene-chloroform as the moving phase to give 17a,21 nene-3 ,1 1,20-trione.

A solution of 45 mg. of 3,20-bis-semicarbazido-17a,21- dihydroxy-16a-methyl-4-pregnene 3,11,20 trione 21-acetate, 17 mg. of sodium borohydride, 1 ml. of tetrahydro- -furan and 1.3 ml. of water is maintained at reflux temperature for approximately one hour. The reaction solution is cooled to about 15 decomposed by the addition of a solution of 27 mg. of glacial acetic acid in 0.2 ml. of water. The tetrahydrofuran is evaporated in vacuo, and the residual material is extracted with ethyl acetate. The ethyl acetate extracts are washed with a saturated salt solution, water, 5% aqueous sodium bicarbonate solution and again with Water. The extracts are dried and the ethyl acetate evaporated in vacuo to give 3,20 bis-semicarbazido 11B,17a,21 trihydroxy-16a-methyl-4-pregnene-3,20-dione.

A mixture of 60 mg. of 3,20-bis-semicarbazido-1l6, 17a,21 trihydroxy-16a-methyl-4-pregnene-3,20-dione, 0.2 ml. of dimethylformamide, 0.6 ml. of chloroform, and 1.5 ml. of 1.0 N aqueous hydrochloric acid is heated under reflux for a period of about three hours. The resulting two-phase system is cooled to a temperature of approximately 15 C., and the layers are separated. The aqueous layer is extracted with chloroform, and the chloroform extracts are combined with the original chloroformdimethylformamide solution. The combined organic layer is washed with an aqueous solution of sodium bicarbonate, and the chloroform and dimethylformamide in the combined organic layer is replaced with ethyl acetate by evaporation in vacuo. Petroleum ether is added and the resulting solution is subjected to a partition chromatogram using aqueous methanol as the stationary phase and benzenechloroform as the moving phase to give 11 3,17a,21-trihydroxy-16ot-methyl-4-pregnene-3,20-dione. The latter mais extracted with chloroform,

dihydroxy 16m methyl-4-preg- C., and the excess sodium borohydride terial is reacted with an excess of acetic anhydride in pyridine at room temperature for a period of about fifteen hours, and the crude acetylated product is recrystallized from ethyl acetate to give 11 3,17a,21-tri'hydroxy-16amethyl-4-pregnene-3,20-dione 2l-acetate.

To a cooled solution of 600 mg. of 11 3,l7a,21-trihydroxy-l6a-methyl-4-pregnene-3,20-dione ZI-acetate in 5.0 ml. of dry pyridine is added 1.15 ml. of phosphorous oxychloride, and the mixture is allowed to stand at room temperature for a period of approximately 15 hours. The reaction solution is evaporated in vacuo at a temperature of about 20 C. to a volume of 23 ml. Seventeen milliliters of Water is added slowly to the concentrated solution, with stirring, and the aqueous mixture is extracted with ethyl acetate. The combined ethyl acetate extracts are washed with water, then with dilute aqueous hydrochloric acid solution, again with water, and then with a dilute aqueous sodium bicarbonate solution. The washed ethyl acetate solution is dried, and the solvent is evaporated in vacuo; the residual material is triturated with ether, and the crystalline material is recrystallized from ethyl acetate-ether to give 17u,21-dihydroxy-16u-methyl- 4,9(11)-pregnadiene-3,20-dione 21-acetate. A suspension of 330 mg. of 17a,2l-dihydroxy-l6a-methyl-4,9(11)- pregnadiene-3,20-dione 21-acetate and 1.8 g. of N-bromosuccinimide in a mixture of 50 ml. of dioxane and 10 ml. of water is cooled to 10 C. Then with stirring, 10 ml. of cold 1.0 N aqueous perchloric acid is added. The temperature of the reaction mixture is allowed to rise to 15 C. and is maintained at this point for about two and one-half hours during which time the solid material slowly dissolves. The resulting yellow solution. is treated with 1.0 ml. of allyl alcohol to discharge the color and decompose the remaining N-bromo-succinimide, and the resulting solution is evaporated to a small volume in vacuo. The concentrated solution is diluted with water, and the aqueous mixture is extracted with ethyl acetate. The ethyl acetate extracts are washed, dried and evaporated to dryness, and the residual material is crystallized :from ethyl acetateether to give 911 bromo 11fl,17a,21 -trihydroxy 16a methyl-4-pregnene-3,20-dione 21-acetate.

A solution of 210 mg. of 9a-bromo-11fl,17u,21-trihydroxy-l6ot-methyl-4-pregnene-3,20-dione 21-acetate and 240 mg. of potassium acetate in 10 ml. of absolute ethanol is heated under reflux for two hours. The reaction mixture is cooled to room temperature, and evaporated in vacuo to a small volume. The concentrated aqueous mixture is extracted with three portions of ethyl acetate, and the combined ethyl acetate extracts are washed with water, dried, evaporated to dryness in vacuo. The residual material is crystallized from 3,20-dione 21-acetate. To a solution of 83 mg. of anhydrous hydrogen fluoride in 4.7 ml. of ice-cold alcoholfree chloroform is added an ice-cold solution of 416 mg. of 95,116 epoxy 17a,2l dihydroxy-16otmethyl-4-preg-- nene-3,20-dione 21-acetate. The solution is mixed thoroughly and maintained at 0 C. for two hours, at the end of which time 13.0 ml. of ice-cold 20% aqueous sodium acetate is added, and the resulting mixture agitated vigorously. The layers are separated,'and the chloroform layer is washed with water until free of acid, dried, and the chloroform evaporated in vacuo. The residual material is crystallized from acetone-petroleum ether to give 91x fluoro-l 1B,17a,21-trihydroxy-16a-rnethy1-4-pregnene- 3,20-dione 2l-acetate. Fifty milligrams of a -fluoro- 11B,17a,21-trihydroxy 16cc methyl 4 pregnene 3,20- dione 21-acetate is dissolved in a mixture of 1.0 cc. of

1 N methanolic potassium hydroxide, and the solution is ethyl acetate-ether to give 95,115 epoxy-17a,21-dihydroxy-16a-methyl-4-pregnene- A solution of 400 mg. of 9oc-fluOr011[3,17a,21-trihydroxy-16ix-methyl-4-pregnene-3,20-dione 21-acetate in 4 ml. of pyridine is added to the complex formed by the addition of 400 mg. of chromium tri-oxide to 4 ml. of pyridine. The mixture is swirled until thoroughly mixed and then allowed to stand at room temperature overnight. The reaction mixture is poured into water, and the aqueous mixture is extracted with ether and then twice with ethyl acetate. The combined ether and ethyl acetate extracts are washed with dilute aqueous sulfuric acid at about C., and then with water until neutral. The organic solvent layer is then dried, the solvents are evaporated therefrom in vacuo, and the residual crystalline material is purified by crystallization from ethyl actate-ether to give 9a fluoro-17a,21-dihydroxy-l6u-methyl-4-pregnene- 3,11,20-trione 21-acetate. Fifty milligrams of 90t'flUO1'O- 17oc,2l dihydroxy l6ot-methyl-4-pregnene-3,l1,20-trione ZI-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about ten minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is crystallized from ethyl acetateether to give 9a-fiuoro-17a,21-dihydroxy-16a-methyl-4- pregnene-3,11,20-trione.

To a solution of 110 mg. of 17a,2l-dihydroxy-16amethyl-4-pregnene-3,11,20-trione 21-acetate in 6 ml. t-butanol, 0.01 ml. glacial acetic acid and 0.03 ml. of acetic anhydride is added 70 mg. of selenious acid (H SeO The mixture is heated to the boiling point overnight, another 50 mg. of selenious acid is added, and the heating is continued for an additional 24 hours. The solution is decanted from metallic selenium and evaporated to an oil which is then dissolved in ethyl acetate. The ethyl acetate solution is washed with aqueous sodium bicarbonate and then with water until neutral, and dried. The solvent is evaporated from the dried solution to give an oil which is dissolved in benzene and adsorbed from this solvent on acid-washed alumina. The adsorbate is eluted with ether-petroleum ether and then with mixtures of ether and choloroform, increasingly rich in chloroform. The 4:6 ether-chloroform eluates are combined, evaporated to dryness, and the residual material recrystallized from ethyl acetate-ether to give 17a,21-dihydroxy-1Ga-methyl-l, 4- pregnadiene-3,11,20-trione 21-acetate; M.P. 208212 C. Fifty milligrams of 17u,21-dihydroxy-16u-methyl-1,4- pregnadiene-3,11,20-trione 21-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about ten minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is crystallized from ethyl acetate-ether to give 17a-21-dihydroxy-16a-methyl-1,4-pregnadiene,3,1l-20-trione.

To a solution of 100 mg. of 11;3,17a,21-trihydroxy-16umethyl-4-pregnene-3,20-dione 21-acetate in 6 ml. t-butanol, 0.01 ml. glacial acetic acid and 0.03 ml. of acetic anhydride is added 70 mg. of selenious acid. The mixture is heated to the boiling point overnight, another 50 mg. of selenious acid is added, and the heating is continued for an additional 24 hours. The solution is decanted from metallic selenium and evaporated to an oil which is then dissolved in ethyl acetate. The ethyl acetate solution is washed with aqueous sodium bicarbonate and then with water until neutral, and dried. The solvent is evaporated from the dried solution to give an oil which is dissolved in benzene and adsorbed from this solvent on acid-washed alumina. The adsorbate is eluted with ether-petroleum ether and then with mixtures of ether and chloroform, increasingly rich in chloroform. The 4:6 ether-chloroform eluates are combined, evaporated to dryness, and the residual material recrystallized from ethyl acetate-ether to give 11B,17a,21 trihydroxy-16a-methyl-1,4-pregnadiene- 3, 20-dione Zl-acetate. Fifty milligrams of l1B,17a,21-trihydroxy-16a-methyl 1,4 pregnadiene-3,20-dione 21-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about ten minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is crystallized from ethyl acetate-ether to give 11B,17a,21 trihydroxy 16u-methyl-1,4-pregnadiene-3,20-dione.

To a solution of 110 mg. of 9a fluoro 170;,21 dihydroxy 16a methyl 4 pregnene 3,11,20 trione 21-acetate in 6 ml. t-but-anol, 0.01 ml. glacial acetic acid and 0.03 ml. of acetic anhydride is added 70 mg. of selenious acid (H SeO The mixture is heated to the boiling point overnight, another 50 mg. of selenious acid is added, and the heating is continued for an additional 24 hours. The solution is decanted from metallic selenium and evaporated to an oil which is then dissolved in ethyl acetate. The ethyl acetate solution is washed with aqueous sodium bicarbonate and then with water until neutral, and dried. The solvent is evaporated from the dried solution to give an oil which is dissolved in benzene and adsorbed on activated alumina. It is eluted with ether-petroleum ether and then with mixtures of ether and chloroform, increasingly rich in chloroform. The 4:6 etherchloroform eluates are combined, evaporated to dryness, and the residual material recrystallized from ethyl acetate ether to give 9a fluoro 17a,21 dihydroxy 160w.

methyl 1,4 pregnadiene 3,11,20 trione 21 acetate. Fifty milligrams of 9a fluoro 1704,21 dihydroxy 16amethyl 1,4 'pregnadiene 3,11,20 trione 21 acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about ten minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is crystallized from ethyl acetate-ether to give fluoro 170:,21 dihydroxy 16a methyl- 1,4 pregnadiene 3,11,20 trione.

To a solution of mg. of 9a fluoro 11B,17a,21- trihydroxy 16a 5 methyl 4 pregnene 3,20 dione 21-acetate in 6 ml. t-butanol, 0. 01 ml. glacial acetic acid and 0.03 ml. of acetic anhydride is added 70 mg. of selenious acid. The mixture is heated to the boiling point overnight, another 5-0 mg. of selenious acid is added, and the heating is continued for an additional 24 hours. The solution is decanted from metallic selenium and evaporated to an oil which is then dissolved in ethyl acetate. The ethyl acetate solution is washed with aqueous sodium bicarbonate and then with water until neutral, and dried. The solvent is evaporated from the dried solution to give an oil which is dissolved in benzene and adsorbed from this solvent on acid-washed alumina. The adsorbate is eluted with ether petroleum ether and then with mixtures of ether and chloroform, increasingly rich in chloroform. The 4:6 ether-chloroform eluates are combined, evaporated to dryness, and the residual material recrystallized from ethyl acetate ether to give 90: fluoro- 11,B,17a,21 trihydroxy a methyl 1,4 pregnadiene 3,20 dione 21 acetate. Fifty milligrams of 9a fluoro 11B,17a,21 trihydroxy 16a methyl 1,4- pregnadiene 3,20 dione 21 acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about ten minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is crystallized from ethyl acetate-ether to give 90:- fluoro 11fl,17u,21 trihydroxy 16cc methyl 1,4- pregnadiene-SJO-dione.

In a 500 ml. 3-neck flask equipped with condenser, dropping funnel and nitrogen inlet are placed 20' g. of potassium hydroxide in 90 ml. of water, 100 ml. of methanol and 100 ml. of ether. A solution of 1 0 g. of N-methyl- N-nitrosotosylamide in 50 ml. of ether is placed in the dropping funnel.

Diazomethane is generated by warming the generation flask to 40-45 N-nitrosotosylamide-ether from the drop-ping funnel. Nitrogen is utilized to sweep the diazomethane into a solution of 20 g. of 3a acetoxy 16 pregnene 11,20- dione in 100 ml. of tetrahydrofuran and 120 ml. of ether. The process is continued until the steroid solution remains yellow for several hours. The product, 30: acetoxy- 16m,17or-methyleneazo-preguane 11,20-dione largely precipitates from the reaction mixture. After 16 hours, the mixture is filtered, washed with ether and dried in air. Yield about 14 grams, M.P. 186-l9 C.

37.4 g. of 30c acetoxy 16a,17a methyleneazo pregnane 11,20 dione is placed in a 500 ml. round-bottom flask and heated by an oil bath in vacuo (pressure 0.6 mm). A manometer and 12-liter surge flask are in the line between the reaction flask and pump trap. When the bath temperature reaches 180 C. the 30: acetoxy- 16a,17u methyleneazo pregnane 11,20 dione begins to melt with evolution of nitrogen. The maximum pressure reached is 83 mm. After 10 minutes at 180-182 C. the melt is cooled. It has 249, E percent 191 and is taken up in about 150 ml. of acetone, filtered through diatomaceous earth, concentrated to about 100 ml., and ether is slowly added to the boiling solution until crystallization occurs. These. crystals of 3a acetoxy 16- methyl 1 6 pregnene 11,20 dione weigh about 19.0 g., M.P. 165168 C.'

A solution of 20.0 g. of 3a L acetoxy 1-6 methyl 16- I pregnene 11,20 dione dissolved in 60 ml. of methanol, is cooled to 18 C., and 80 ml. of 30% hydrogen peroxide followed by 8 0 mLof 2.5 N sodium hydroxide are added. Considerable material precipitates from solution, but all redissolves on stirring the reaction mixture at 2530 C. for 40 minutes. The solution is kept at l5-20 C. for 18 hours at which time the ultraviolet maximum at 249 has completely disappeared. Then 600 ml. of saturated salt water'is slowly added, the crystalline precipitate is filtered, washed with water, and dried in air and inhydroxy 16B- formed weighs vacuum; The 16a,17 epoxy 3a,- methyl- -pregnane 5 11,20 dione thus about 17 g.; M.P. 176-177? ,C.; hexagonal prisms M.P.

178180 C. from acetonerether To a solution of 2.69 g. of 16a,17a-epoxy-3a-hydroxyl6B-methyl-pregnane-11,20-dione in 55 ml. dioxane is added.2,7 ml. of 2M aqueous perchloric acid. The clear solution is kept at 2530 C. for 65 hours. Cold water (175 ml.) is added, the slurry chilled to 8 C. and filtered I after 30 minutes. The precipitate, containing a mixture of 306,170C-dlhYdI'OXY 16-methyl 15-pregnene-11,20-dione and 3a,17a-dihydroxy-16-methylene-pregnane-11,20-dione is washed withwater, and dried in air and finally at 50 C. in vacuum. Yield: approximately 2 g.;' M.P. sintering at about 150 C., meltingat 158167 C. The relative tomaceous earth. The colorless filtrate is taken to dryness and crystallized from ether; a mixture of 3a, l 7ot-dihydroxy-16a-methyl-pregnane-11,20-dione and 3u,17ot-dihydroxy-16,B-methyl pregnane 11,20 dione is obtained;

C. and cautiously adding the N-methyl-.

zene gives 17u,21-dihydroxy-16 8-methyl 14 weight about 3 g., sintering at 150 melting at 166 182 C.

The product consists of 3a,17a-dlihydroxy-16u-methylpregnane-11,20-dione and 3a,17ix-dihydroxy-16,3-methylpregnane-11,20-dione in the ratio ca. 7:3 as determined by the amounts of end product isolated below.

One gram of this hydrogenation product containing 3a,17a-dihydroxy-l6a-methyl pregnane-ILZO-dione and 3a,17a-dihydroxy-16fl-methyl pregnane-11,20-dione, is chromatographed on 100 g. of activi'tated magnesium silicate. The 100% chloroform eluates give 3a,17a-dihydroxy-lGa-methyI-pregnane-I1,20-dione, M.P. 188191 C. The 5% methanol-chloroform eluates :give 3a,17'u-di hydroxy-16fimethyl pregn ane 11,20-dione, hexagonal plates from benzene-ethylacetate; M.P. 192-197 C.

A solution of 3.50 g. (9.7 rnillimols) of 3a,17a-dihy droxy-16fi-methyl-pregnane-l1,20-dione in '40 ml. of chloroform is warmed to 40-45 C. A solution of 1.76 .g. (11 millimols) of bromine in 25 ml. of chloroform is added dropwise to the stirred solution such that the color is not darker than pale yellow (ca. 2 drops/see, total time 1 hour). The nearly colorless solution is cooled to 20 C. and 200 ml. of ether is added. The mixture is extracted with excess cold 5% potassium bicarbonate solution, sodium bisulfite solution, and Water, and dried over magnesium sulfate. The colorless residue after removal of sol- 'vent, 2l-bromo-3a,17u-dihydroxy-16 8-methy1 pregnane- 11,20-dione (about 4 grams) gives a positive tetrazolium test.

To 4.30 g. of 21bromo-3a,17a-dihydroxy-16fi-methylpregnane-11,20-dione in ml. of acetone and 0.01 ml. of acetic acid is added 4.83 g. of anhydrous potassium acetate and'3.85 g. of potassium iodide. The stirred mixture is refluxed for 1 8 hours and concentrated on the water pump to a small volume. Water is added, the product extracted int-o ethyl acetate, and the organic extract dried over magnesium sulfate to give about 4 grams of a colorless foam that partly crystallizes from acetone-ether to give 3a,17a,21trihydroxy-16,8-methyl pregnane-11,20- dione 2l-acetate.

To a solution of 3a,17a,2l-trihydroxy-16fl-methyl-preg-- nane-11,20-dione ZI-acetate (4.0 g.) in ml. t-but-anol' and 20 ml. of water cooled to 10-15 C., is added 3.5 g. N-bromosuccinirnide. The suspension is stirred at 15 C. until all the N-bromosuccinimide has dissolved (90 minutes). The reaction mixture is kept at 2 C. for about sixteen hours and at 25 C. for 2 hours. Sodium sulfite solution is added to destroy bromine and the mixture concentrated on the water pump to a low volume. A granular precipitate forms; water is added, the precipitate filtered and washed with water; chromatography on neutral alumina and elution with mixtures of chloroform and benpregnane-3,1 1, 20-trione ZI-acetate, M.P. 210-213 C.

To a stirred solution of 585 mg. of 1,7a,21-dihydroxy- 16,6-methyl-pregnane-3,11,20-trione 21-acetate in 10 ml. of acetic acid and 8 ml. of chloroform kept at 10 C. is

added slowly 230 mg. of bromine in 6 ml. of chloroform. After addition is complete, 1.2 g. of sodium acetate in 7 ml. of cold water is added and the mixture is extracted with chloroform. The chloroform extract is washed with dilute potassium bicarbonate, water and dried over sodium sulfate. The residue is triturated with ether to give 480 mg. of crystalline 4bromo-17a,21 dihydroxy- 16/8-methyl-pregnane3,11,20-trione 21.-acet-ate, M.P. C. dec.

To 583 mg. of 4-bromo-17a,21-dihydroxy-16fl-methylpregnane-3,11,20-trione 21-acetate in 20 ml. of acetonitrile under nitrogen is added a slurry of 600 mg. of semicarbazide hydrochloride and 410 mg. sodium bicarbonate in 4 ml. of water. After 2 hours, the acetonitrile is removed in vacuo, water is added and about 540 mg. of crystalline 3-semicarbazone of l7a,21-dihydroxy-165 15 methyl-4-pregnene-3 ,1 1,20-trione washed with Water and dried.

540 mg. of the 3-semicarbazone of l7ot,2l-dihydroxy- 1613-methyl-4-pregnene-3,l1,20-trione 2l-acetate is dissolved in 20 ml. of acetic acid, 1.5 ml. of pyruvic acid and 5 ml. of water. After 18 hours at 25 C., water is added and the mixture extracted with chloroform. The chloroform extract is washed with aqueous potassium bicarbonate, water and dried over sodium sulfate. Removal of solvent gives crude 17a,2ldihydroxy-16fl-methyl-4-pregnene-3,11,20-trione 2l-acetate which is purified by chromatography on neutral alumina and crystallization from acetone-ether (hexagonal plates). The pure material has M.P. 226-232" C. 100 mg. of 17a,2l-dihydroxy-16[3- methyl-4-pregnene-3,11,20-trione 2l-acetate in 3 ml. of methanol is treated with 0.1 g. of potassium bicarbonate in 1 ml. of water, the methanol is evaporated in vacuo, and the residual material is extracted with ethyl acetate. Evaporation of the ethyl acetate solution gives crystalline l7a,2l di'hydroxy-l6,6-methyl-4-pregnene-3,l1,20-trione.

To a stirred solution of 500 mg. of 17u,21-dihydroxy- 16 3-methyl-4-pregnene-3,11,20-trione 21-acetate in 12.5 ml. of methanol and 3 ml. of dimethylformamide kept under nitrogen is added a slurry of 680 mg. of semicarbazide hydrochloride and 370 mg. of sodium bicarbonate in 1 ml. of water. The stirred mixture is refluxed 3 /2 hours and maintained at 45 C. for 17 hours. It is then cooled to 20 C. and 50 ml. of 50% saturated aqueous sodium chloride is added. After 2 hours at C. the precipitate of 3,20-bis-semicarbazido-17a,21-dihydroxy-16flmethyl-4-pregnene-3,11,20-trione 2l-acetate is filtered, washed with water until free of chloride ion and dried in To a stirred solution of 600 mg. of 3,20-bis-semicarbazido-l7ot,2l-dihydroxy-l6fi-methyl-4-pregnene 3,11,20- trione 21-acetate in 30 ml. of tetrahydrofuran and 11 ml. of water under nitrogen is added 200 mg. powdered sodium borohydride. The stirred suspension is refluxed 45 minutes and then cooled to 15 C. Aqueous acetic acid (3 ml. of 30%) is added cautiously and most of the tetrahydrofuran is removed in vacuum. Addition of ml. of methanol and 5 ml. of water induces the product to crystallize. Following addition of ml. of a saturated sodium chloride solution and aging at 0 C. the product 3,20-bissemicarbazido-l1/3,17u,21-trihydroxy-16fl-methyl-4 pregnene-3,20-dione is filtered, washed with water, and dried 1n air.

To a solution of 510 mg. of reduced 3,20-bis-semicarbazido-l1B,17a,21-trihydroxy-16B-methyl-4-pregnene 3, 20-dione in 5 ml. of acetic acid is added 1.20 ml. of water and 0.50 ml. of pyruvic acid. The solution is kept at 25 C. for eighteen hours. Water (20 m1.) is added, and the mixture is extracted thoroughly with chloroform. The chloroform extract is dried over magnesium sulfate and taken to dryness. The residue is crystallized from acetoneether to give pure 116,17 a,2ltrihydroxy-l6B-methyl-4- pregnene-3,20-dione. A olution of 100 mg. of l1B,l7 x,2ltrihyd-roxy-16B-methyl-4-pregnene-3,20-dione in 1.0 ml. of pyridine and 0.5 ml. of acetic anhydride is prepared. After 18 hours at 25 C., the solution is taken to dryness in vacuo and the solid residue purified by crystallization from acetone-ether to give l1,8,17a,2l-trihydroxy-l6fimethyl-4-pregnene-3,20-dione 21-acetate.

A solution of 400 mg. of 1lfi,l7u,2l-trihydroxy-l6[3- methyl-4-pregnene-3,20-dione 21-acetate in 2.0 ml. dimethyl formamide, 0.8 ml. of pyridine and 0.4 ml. of methanesulfonyl chloride is kept at 75 C. for one hour. The mixture is cooled, water added, and the precipitate filtered, washed with water and dried in air. The desired 1711,21 dihydroxy-l6,B-methyl-4,9(ll)-pregnadiene-3,20- dione 21-acetate is purified by chromatography on alumina (20 g.) and elution of the column with benzene. Crystallization of material eluted by benzene gives pure 17a,2ldihydroxy-l6p-methyl-4,9(11)-pregnadiene-3 ,ZO-dione 21- acetate.

2l-acetate filtered,

To a mixture of 620 mg. of 17a,21-dihydroxy-l65- methyl-4,9(11)-pregnadiene-3,20-dione 2l-acetate and 330 mg. of N-bromosuccinimide in l0 ml. of dio-xane and 3.2 ml. of water cooled to 10 C. is added 1.8 ml. of cold 1 M aqueous perchloric acid. The mixture is stirred at 15 C. for 3 hours. Excess N-bro'mosuccinimide is destroyed by addition of aqueous sodium thiosulfate and most of the dioxane is removed in vacuo. About 30 ml. of water is added and crystalline bromohydrin, 9a-bromo- 11,8,17oc,21 trihydroxy-16fi-methyl-4-pregnene-3,20-dione 21-acetate, is filtered, washed with water, and dried in air.

To the stirred solution of mg. of the 9a-bromo-1lfi, 17u,21-trihydroxy-16,8-methyl-4-pregnene-3,20 dione 21- acetate in 3 ml. of tetrahydrofuran and 1 ml. of methanol under nitrogen is added 1.02 ml. of 0.215 N methanolic sodium methoxide. After 10 minutes at 25 C., 0.2 m1. of acetic acid is added and the methanol removed in vacuo. The residue is acetylated with 1.00 ml. of pyridine and 0.5 ml. of acetic anhydride at 60 C. for 70 minutes. The mixture is taken to dryness in vacuo, water added, and the product extracted into chloroform. The residue is crystallized from ether-acetone to give pure 9,8,11,8- epoxy-17a,21-dihydroxy 16/3 methyl-4-pregnene-3,20- dione 21-acetate.

To a solution of 200 mg. of 9fl,11fi-epoxy-17a,21-dihydroxy-l6fi-methyl-4-pregnene-3,20-dione 21-acetate in 2 ml. of chloroform and 2 ml. of tetrahydrofuran in a polyethylene bottle at 60 C. is added 2 ml. of a 2:1 (by weight) mixture of anhydrous hydrogen fluoride and tetrahydrofuran. After 4 hours at 10 C. the mixture is cooled to 60 C. and cautiously added to a stirred mixture of 30 ml. of 25% aqueous potassium carbonate and 25 ml. of chloroform kept at 5 C. The aqueous phase is further extracted with chloroform and the latter phase washed with water and dried over magnesium sulfate. The residue on crystallization from acetone-ether gives pure 9u-fluoro-11 3,17a,21 trihydroxy-lofl methyl 4- pregnene-3,20-dione 2l-acetate.

To a stirred solution of mg. of 9ot-fil1OIO-1l]3,17u, 2l-trihydroxy 16/3 methyl-4-pregnene 3,20-dione 21- acetate in 5 ml. of methanol under nitrogen at 25 C. is added 1.00 ml. of 0.26 M methanolic sodium methoxide. After 15 minutes, 0.2 ml. of acetic acid in 1 ml. of water is added and the mixture concentrated nearly to dryness. The residue is taken up in ethyl acetate and the ethyl acetate solution is washed with water, dried over magnesium sulfate, and concentrated to dryness. Crystallization of the residue from ethyl acetate gives pure 9a-fluoro- 1 1B, 1701,2l-trihydroxy-l65-methyl-4-pregnene-3 ,20-dione.

To a solution of 100 mg. of 9B,11;8-epoxy-17a,21-dihydroxy-16fl-methyl-4-pregnene-3,20-dione 21-acetate in 4 ml. of cholorform is added 5 ml. of concentrated hydrochloric acid. The two-phase mixture is stirred at 25 C. for 1 hour. Addition of water and chloroform extraction gives a crude crystalline product which is partly de- I acetylated. Treatment with 1 ml. of pyridine and 0.5 ml. of acetic anhydride at 25 C. for 18 hours followed by concentration in vacuo and crystallization of the residue from acetone-ether aflords pure 9a-chloro-11/8,17a,21- trihydroxy-16/8-methyl-4-pregnene 3,20 dione 21-acetate. This compound is hydrolyzed by treatment with potassium bicarbonate in aqueous methanol to give 90:- chloro-115,17a,21 trihydroxy-16B methyl-4-pregnene- 3,20-dione.

To a stirred solution of 682 mg. of l7a,21 -dihydroxy- -methyl-pregnane-3,l1,20-trione 21-acetate in 20 ml. of chloroform and 2.25 ml. of acetic acid maintained at 20 C. is added dropwise one-half of a solution of 540' mg. of bromine in 2 ml. of chloroform and 3 ml. of acetic acid. The mixture is warmed to 0 C. and the remainder of the bromine added. Sodium acetate (0.4 g.) in 2 ml. of water is added followed by 20 mg. of sodium sulfite. The mixture is concentrated in vacuo to remove the chloroform and 20 ml. of water is added. The white 17 powdery precipitate of 2,4-dibromo-17u,21-dihydroxyl6fl-methyl-pregnane-3,11,20-trione 21-acetate is filtered, washed with water and dried in air. Yield: 920 mg, M.P. 122'130 C. dec.

To a solution under nitrogen of 900 mg. of the2,4-di- 'bromo-l7a,21-dihydroxy-16fl-methyl pregnane-3,1l,20- trione ZI-acetate in 5 ml. dimethyl tformamide is added 200 mg. of sodium bromide. After 1 hour at 25 C., 1 ml. of dimethylaniline is added and themixture maintained at 135 C. for 2 /2 hours. The mixture is cooled, added dropwise to dilute hydrochloric acid, and solid crude product filtered, washed with dilute hydrochloric acid, Water and dried in air. Treatment with charcoal, followed by crystallization from acetone gives l7u,21-dihydroxy-l6B-methyl-1,4-pregnadiene 3,l1,20-trione 2l-acetate, M.P. 230 -233 C.

1.0 g. of l7a,21-dihydrox y-16B-methyl-1,4-pregnadiene- 3,11,20-trione 2l-acetate in 30 ml. of methanol is treated with 1 g. of potassium bicarbonate in 10 m1. of water under nitrogen at reflux temperature for 7 minutes. The mixture is cooled, neutralized with 1 ml. of acetic acid in 10 ml. of Water, the methanol removed in vacuo and the product' extracted into ethyl acetate. Removal of the ethyl acetate gives crystals (about 0.9 g.) of the desired 17a,21-dihydroxy-16/3-methyl 1,4 pregnadiene-3,11,20- trione; M.P. l95-200 C.

To 100 mg. of 11B,17u,21-trihydroxy 16;? methyl- L pregnene-3,20-dione 2l-acetate in 5 ml. of acetic acid is added 50 mg. of selenium dioxide. The mixture is refluxed under nitrogen 18 hours, 50 mg. of selenium dioxide is added and the mixture refluxed an additional 24 hours. The mixture is filtered, and the filtrate taken to dryness. The residue is taken up in ethyl acetate and washed successively with aqueous sodium bicarbonate, ammonium sulfide, dilute ammonia water, water, dilute hydrochloric acid and water and dried over magnesium sulfate. It is then treated with activated charcoal and concentrated to dryness. Crystallization of the residue from acetone-ether gives pure 1lB,l7u,21-trihydroxy-16B-methyl-L4-pregnadiene-3,20-dione 2l-acetate. 100 mg. of 11fi,17a,2l-trihydroxy-l6fl-n1ethyl-l,4-pregnadiene-3,20-dione 21 acetate in 3 ml. of methanol is treated with 0.1 g. of potassium bicarbonate in 10 m1. of water under nitrogen at reflux temperature for 7 minutes. The mixture is-cooled, neutralized with 0.1 ml. of acetic acid in 1 ml. of water, the

methanol is evaporated in vacuo and the residual material is extracted with ethyl acetate. Evaporation of the ethyl acetate gives crystalline 11B,170:,21-tfihYdlOXY-16B- methyl-1,4-pregnadiene-3,20-dione.

In a similar manner, 100 mg. of 9oc-fiL10I0-11B,17cc,21--

trihydroxy-l68-rnethyl-4-pregnene-3,20-dione ZI-acetate is treated with selenium dioxide to produce the corresponding 9iz-fluoro l1fi,17a.21 trihydroxy-16B-methyl- 1,4-pregnadiene-3,20-dione ZI-acetate. This compound is hydrolyzed with potassium bicarbonate in aqueous methanol in accordance with the procedure described in the preceding paragraph to give 9a-fluoro-11B,17a.21 trihydroxy-l6fi-methyl-l,4-pregnadiene-3.20-dione. Similarly, 100 mg. of 9a-chloro-1lB,l7et.21-trihydroxy-lGB-methylr 4-pregnene-3,20-dione 2l-acetate is treated with selenium dioxide to produce 9ot-chloro-l1l9,17a,21-trihydroxy-16B- methyl-l,4-pregnadiene-3,20-dione 2l-acetate, which is hydrolyzed by treatment with potassium bicarbonate in aqueous methanol to give 9wchloro-11/i,17ot,21-trihydroxy-16fi-methyl-1.4pregnadiene-3,20-dione;

A solution of 100 mg. of 9a-fluoro-11B,17 x.21-trihydroxy-l6fi-methyl-1,4-pregnadiene-3,20-dione Ill-acetate in 1 ml. of pyridine is added to the complex formed by the addition of 100 mg. of chromium trioxide to 1 ml.

of pyridine. The mixture is swirled until thoroughly mixed and then allowed to stand at room temperature overnight. The reaction mixture is poured into water, and the aqueous mixture is extracted with ether and then twice with ethyl acetate. The combined ether and ethyl acetate extracts are washed with dilute aqueous sulphuric acid at about 0 C., and then with water until neutral. The organic solvent layer is then dried, the solvents are evaporated therefrom in vacuo, and the residual crystalline material is purified by crystallization from ethyl acetateether to give 9a-fluoro-17a,21-dihydr0xy-l6fi-methyl-L4 pregnadiene-3,11,20-trione ZI-acetate. This compound is hydrolyzed by treatment with potassium bicarbonate in aqueous methanol to form 9a-fiuoro-17a,2l-dihydroxyl6fl-methyl-1,4-pregnadiene-3,l 1,20-trione.

In a similar manner, 9u-chloro-11B,17a,2l-trihydroxyl6,8-methyl-1,4-pregnadiene-3,20-dione 21-acetate is reacted with chromium trioxidepyridine complex to give 9a-ch1oro 17a,21 dihydroxy-l6B-methyl-1,4-pregnadiene-3,11,20-trione 2l-acetate, which is hydrolyzed by treatment with potassium bicarbonate in aqueous methanol to give 9ot-chloro-17a,2l-dihydroxy-l6fl-methyl-1,4- pregnadiene-3,11,20-trione.

Similarly, 9u-fiuoro-l1,8,l7a,2l-trihydroxy-16fl-methyl- 4-pregnene-3,20 iione ZI-acetate is reacted with chromium trioxide-pyridine complex to form 9a-fluoro-l7u,2ldihydroxy-16B-methyl 4-pregnene-3,11,20-trione 21-acetate which is hydrolyzed by treatment with potassium bicarbonate in aqueous methanol to produce 9a-fluoro- 171,2l-dihydroxy-16,8-methyl-4-pregnene-3,11,20-trione.

Similarly, 9a-chloro-1 1p,17bt,21-trihydroxy-16B-methyl- 4-pregnene-3,20-dione 2l-acetate is reacted with chromium trioxide-pyridine complex to form c-ChlOrO-17oc, 21 dihydroxy-16,8-methyl-4-pregnene-3,11,20-trione 21- acetate which is hydrolyzed by treatment with potassium bicarbonate in aqueous methanol to produce 9a-ChlQIO- 17a,21-dihydroxy-16B-methyl-4-pregnene-3,11,20-trione.

10 grams of 17vt,2l-dihydroxy-16a-methyl-4-pregnene- 3,11,20-trione which can be prepared as described hereinabove, are dissolved in 400 cc. of chloroform. To this solution is added a mixture of cc. of concentrated aqueous hydrochloric acid. and 100 cc. of 37% aqueous formaldehyde solution. The resulting mixture is stirred for a period of approximately 3 days at room temperature. The chloroform layer is separated, washed with sodium bicarbonate solution until neutral, then with water, dried over anhydrous sodium sulfate, and evaporated to dryness in vacuo. The residual crude material is purified by crystallization from a mixture of methylene chloride and methanol to give l7tx,20,20,2l-bismethylenedioxy-16a-methyl-4-pregnene-3,1 l-dione.

10 grams of 17a,20,20,21-bisrnethylenedioxy-16amethyl-4-pregnene-3,1l-dione are dissolved in 500 cc. of benzene, to the solution is added 25 cc. ethylene glycol and 1 gram of p-toluenesulfonic acid, and the resulting mixture is heated under reflux for a period of approximately 15 hours. The reaction solution is cooled, washed with aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and evaporated to dryness in vacuo. The residual crude material is absorbed from its solution in benzene on 250 g. of acid-washed alumina, and the resulting adsorbate is eluted utilizing mixtures of ether-petroleum ether to give 3-ethylenedioxy-17ot, 20,20, 2 l-bismethylenedioxy- 1 6a-methyl-5-pregnene-l l-one.

A mixture of 10 grams of 3-ethylenedioxy-17-a, 20,20, 21-bismethylenedioxyl6a-methyl-5-pregnene-l l-one, 4.3 g. perbenzoic acid and 230 cc. benzene is allowed to stand at room temperature for a period of about 2 days. A portion of the epoxide product, which precipitates, is separated from the reaction solution by decantation, and the decanted solution is washed with saturated aqueous sodium bicarbonate solution and then dried over anhydrous sodium sulfate. The dried solution is then evaporated in vacuo, and the residual epoxide product is combined with. the epoxide product originally separated from the reaction mixture.

allowed to stand at room temperature for a period of about 2 hours. The reaction solution is poured into water, and the aqueous mixture is extracted with chloroform. The chloroform solution is Washed with saturated aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and evaporated in vacuo to give a mixture of 17a, 20,20,21-bismethylenedioxy-5-hydroxy- 16a-methyl-6-formyloxy-pregnane-3,1l-dione and 17,20, 20,21 bismethylenedioxy 6-hydroxy-16a-methyl-5-formyloxy-pregnane-3 ,11dione.

This mixture of S-formyloxy and 6-formyloxy derivatives is dissolved in about 850 cc. of methanol, to this solution is added a solution containing about 17 grams of potassium hydroxide in 80 cc. of water, and the resulting mixture is heated under reflux in a nitrogen atmosphere for a period of approximately /2 hour. The reaction solution is cooled, neutralized with about 23 cc. of acetic acid and evaporated in vacuo to a small volume. The concentrated solution is poured into water and the aqueous mixture is extracted with chloroform. The chloroform extract is washed with aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and evaporated to dryness in vacuo. The residual material is crystallized from methanol to give 17a, 20,20,21-bismethylenedioxy-l6amethyl-allopregnane-3,6,1 l-trione.

A solution containing about 5 grams of 17oc,20,20,21- bismethylenedioxy 16a methyl allopregnene 3,6,11- trione and 0.1 g. of p-toluenesu'lfonicacid in 120 cc. butanone dioxulane is heated under reflux for a period of about 10 minutes. The reaction solution is cooled to about -5 C., diluted with chloroform, and the resulting solution is washed with aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. The resulting dried solution is evaporated to dryness in vacuo, and the residual material is slurried with ether, recovered by filtration and then dried to give 3-ethylenedioxy- 17a,20,20,21 bismethylenedioxy 16a methyl-allopregnane-6,1l-dione.

A solution containing about 5 grams of 3-ethylenedioxy- 17a,20,20,21-bismethylenedioxy-16a-methyl-allopregnane- 6,11-dione in 70 cc. of benzene is added, with stirring over a period of approximately minutes, to an ethereal solution containing the methyl magnesium iodide, prepared from 5 cc. of methyl iodide and 0.5 gram of magnesium turnings, dissolved in 50 cc. of ether. The reaction mixture is allowed to stir for an additional /2 hour period, and the resulting solution is decomposed with 70 cc. of water. About 170 cc. of benzene is added to the aqueous mixture andvthe layers are separated. The aqueous layer is extracted with two 100 cc.-portions of chloroform, and the organic layers are combined, dried over anhydrous sodium sulfate, and evaporated to dryness in vacuo to give 3 ethylenedioxy 17a,20,20,21-bismethylenedioxy-ofl-hydroxy-6u,16a-dimethy1allopregnane-1 l-one.

A solution containing 5.5 cc. of freshly distilled thionyl chloride in 26 cc. of cold anhydrous pyridine is added dropwise, with stirring, to a solution of 5.0 g. of 3-ethylenedioxy-17a,20,20,21 bismethylenedioxy-6;? hydroxy- 6a,16a-dimethyl-allopregnene 1l-one in 32 cc. of anhydrous pyridine, while maintaining the temperature of the reaction mixture at approximately 40 C. The reaction solution is stirred for an additional 30 minute period following the addition of the thionyl chloride reagent, and the reaction mixture is then cooled to about 05 C. and poured into 180 cc. ice water. The aqueous mixture is extracted with chloroform, and the chloroform extract is neutralized, dried over anhydrous sodium sulfate, and evaporated to dryness in vacuo. The residual material, dissolved in benzene, is chromatographed on 150 grams of acid-washed alumina; elution of the resulting adsorbate with mixtures of petroleum ether and ether gives 3-ethylenedioxy 17a, 20,20,21 bismethylenedioxy 6,1604 dimethyl-5 -pregnene-1 l-one.

A solution containing about 5 grams of 3-ethylenedioxy 17a,20,20,21 bismethylenedioxy 6a,16ot dimethyl-S-pregnene-ll-one, 500 cc. of anhydrous acetone and about 0.5 g. of p-toluenesul-fonic acid monohydrate is allowed to stand for a period of about 15 hours. The reaction solution is poured into water, and the aqueous mixture is extracted with chloroform. The chloroform solution is Washed with aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and the chloroform solution is evaporated to dryness in vacuo. The residual material is crystallized from benzene to give 17oc,20,20,2l bismethylenedioxy 6a,16ot dimethyl 4- pregnene-3,l l-dione.

About 0.1 gram of 17a,20,20,21-bismethylenedioxy-6a, 17a-dimethyl-4-pregnene-3,1l-dione is suspended in 18 cc. of 50% aqueous acetic acid, and the suspension is carefully purged with nitrogen, following which the suspension is heated on a steam bath under nitrogen for a period of about 8 hours and then allowed to stand at room temperature for an additional period of 15 hours. The reaction solution is evaporated to dryness in vacuo to give 17a,2l dihydroxy 60,160c dimethyl 4 pregnenc- 3,11,20-trione. The material is dissolved in 20 cc. of chloroform, and the chloroform solution evaporated to dryness in vacuo. To the residual dry material is added 1 cc. of pyridine and 1 cc. of acetic anhydride, and the resulting mixture is heated on a steam bath for a period of about 15 minutes. The reaction solution is cooled to about 05 C. poured into ice water. The aqueous suspension is extracted with chloroform, and the chloroform extract is washed with aqueous sodium bicarbonate solution, dried over anhydrous soduim sulfate, and evaporated to dryness in vacuo. The residual material, dissolved in 30 cc. benzene, is adsorbed on 5 grams of acid-washed alumina; the adsorbate is Washed with 50 cc. ether. The adsorbate is then eluted with 250 cc. of a 5:5 mixture of ether-chloroform, and then with 50 cc. of a 3:7 mixture of ether-chloroform. The eluates are evaporated in vacuo, and the residual material is crystallized from methanol to give 1711,21 dihydroxy 6oz dimethyl 4- pregnene-3,11,20-triene 21-acetate.

In accordance With the foregoing procedures, but starting with 17a,21-dihydroxy-l6B-methyl-4-pregnene-3,l1,20- triene, there are obtained the corresponding 17a,21-dihydroxy-6a,16,8-dimethyl-4-pregnene-3,11,20-trione and its 21-acetate.

To a solution of 100 mg. of 17a,21-dihydroxy-6a,16adimethyl-4-pregnene-3,11,20-triene 2l-acetate, in 6 ml. tbutanol, and 0.01 ml. of glacial acetic acid is added mg. of selenium dioxide. The mixture is heated under reflux in a nitrogen atmosphere for a period of about 6 hours. The reaction solution is filtered and evaporated in vacuo. The residual material is dissolved in benzene, and the benzene solution is washed with an aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. The benzene solution is stirred with mercury overnight, then centrifuged, and the clear benzene solution is evaporated in vacuo. The residual material thus obtained is separated using partition chromatography on diatomaceous silica (Super-Gel) to give l7oc,2l-dihydroxy-6a,l6udimethyl-1,4-pregnadiene-3,11,20-triene 21 acetate. 40 mg. of 17a,21-dihydroxy-6a,16a dimethyl 1,4 pregnadiene-3,11,20-triene 21-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about 10 minutes. The solution is then acidified with acetic acid, then benzene is evaporated in vacuo, and the residual material is purified by crystallization to give 17a,2l-dihydroxy-6u,16adimethyl-1,4-pregnadiene-3 ,1 1,20-triene.

Similarily, in accordance with the foregoing procedure, but starting with 17a,21-dihydroxy-6u,165-dimethyl-4- pregnene-3,11,20-triene 21-acetate, there are obtained the corresponding 17a,21-dihydroxy 6a,16,8 dimethyl 1,4- pregnadiene-3,11,20-triene, and its 21-ac-etate.

About 5 grams of 3-ethylenedioxy-17a,20,20,21-bismethylenedioxy-6,16m-din1ethyl-5-pregnene-1 l-one, which can be prepared as described hereinabove, is dissolved in about 85 cc. of benzene. This solution is added to a stirred suspension containing 5 grams of lithium aluminum hydride in one liter of anhydrous ether, and the resulting suspension is heated under reflux for a period of about 4 hours. The reaction mixture is allowed to cool to about room temperature, and approximately 33 cc. of ethyl acetate is added to destroy excess lithium aluminum hydride. The resulting mixture is admixed with about 100 cc. of water, the ethereal layer is decanted, and the aqueous layer, diluted With an additional 200 cc. of water, is extracted with chloroform. The ether and chloroform layers are combined, and the combined organic layers are dried over anhydrous sodium sulfate and evaporated to dryness in vacuo. The residual material, dissolved in about 250 cc. of benzene, is adsorbed on about 150 grams of acid- Washed alumina, and the resulting adsorbate is eluted utilizing mixtures of petroleum ether-ether. This eluate is evaporated in vacuo, and the residual material is purified by crystallization from ether to give 3-ethylenedioxy- 170,20,20,2l-bis-methylenedioxy 11B hydroxy 6,1606- dimethyl-5-pregnene.

A solution containing about 5 grams of 3-ethylenedioxy 1706,20,20,21 bismethylenedioxy 1lfl,hydroxy- 6,160t-dimethyl-5-pregnene, 500 cc. of anhydrous acetone and about 0.5 g. of p-toluenesulfonic acid monohydrate is allowed to stand for a period of about 15 hours. The reaction solution is poured into water, and the aqueous mixture is extracted with chloroform. The chloroform solution is washed with aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and the chloroform solution is evaporated to dryness in vacuo. The residual material is crystallized from benzene to give 17a,20,20,21 bismethylenedioxy 11,8 hydroxy 60c, 160t-dimethyl-4-pregnene-3-one.

About 0.1 gram of 170t,20,20,2l-bismethylene-dioxy- 11B hydroxy 60:,160t dimethyl 4 pregnene 3 one is suspended in 18 cc. of 50% aqueous acetic acid, and the suspension is carefully purged with nitrogen, following which the suspension is heated on a steam bath under nitrogen for a period of about 8 hours and then allowed to stand at room temperature for an additional period of 15 hours. The reaction solution is evaporated to dryness in vacuo to give 1'l,8,17a,21-trihydroxy 6a,160t-dimethyl- 4-pregnene 3,20-dione. This material is dissolved in 20 cc. of chloroform, and the chloroform solution evaporated to dryness in vacuo. To the residual dry material is added 1 cc. of pyridine and 1 cc. of acetic anhydride, and the resulting mixture is heated on a steam bath for a period of about 15 minutes. The reaction solution is cooled to about -5 C. and poured into ice water. The aqueous suspension is extracted :with chloroform, and the chloroform extract is washed with aqueous sodium bicarbonate solution, dried over anhydrous sodium sulfate, and evaporated in vacuo. The residual material, dissolved in 30 cc. benzene, is adsorbed on grams of acid-washed alumina; the adsorbate is washed with 50 cc. ether. The adsorbate is then eluted with 250 cc. of a 5:5 mixture of ether-chloroform, and then with 50 cc. of a 3:7 mixture of etherchloroform. The eluates are evaporated in vacuo, and the residual material is crystallized from methanol to give 1l,8,l70,21-trihydroxy-60t,l60t-dimethyl-4-pregnene-3, 20-dione 21-acetate.

In accordance with the foregoing procedure, but starting with 3-ethylenedioxy-17u,20,20,21-bismethylenedioxy- 6,l6B-dimethyl-5-pregnene-ll-one (which is obtained as an intermediate in the preparation of 17a,2l-dihydroxy- 601,165 dimethyl 4 pregnene 3,11,20 trione 21- acetate herein described above). there are obtained the corresponding 1lfi,l70t,2l trihydroxy 60,16B dimethyl-4-pregnene-3,20-dione and its 21-acetate.

To a solution of 100' mg. of 11/3,170t,2l-trihydroxy- 6a,16a-dimethyl-4pregnene-3,20-dione 2l-acetate, in 6 ml. t-butanol, and 0.01 ml. of glacial acetic acid, is added 70 mg. of selenium dioxide. The mixture is heated under reflux in a nitrogen atmosphere for a'period of about 6 hours. The reaction solution is filtered and evaporated in vacuo. The residual material is dissolved in benzene, and the benzene solution is washed with an aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. The benzene solution is stirred with mercury overnight, then centrifuged and the clear benzene solution is evaporated in vacuo. The residual material thus obtained is separated using partition chromatography on diatomaceous silica (Super-Gel) to give ll,B,l7a,2ltrihydroxy 60;,160; dimethyl 1,4 pregnadiene 3,20- dione 2l-acetate. 45 mg. of 1l/i,170t,21-trihydroxy 611,16!!- dimethyl 1,4 pregnadiene 3,20 dione 21-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of l N methanolic potassium'hydroxide, and the solution is allowed to stand at room temperature for a period of about 10 minutes. The solution is then acidified with acetic acid, then benzene is evaporated in vacuo and the residual material is purified by crystallization to give 11fl,170t,21 trihydroxy 600,160t dimethyl 1,4 pregnadiene-3,20-dione.

Similarly, in accordance with the foregoing procedures but starting with 11B,l70,21-trihydroxy-60t,16/3-dimethyl- 4-pregnene-3,20-dione 21-acetate, there are obtained the corresponding 11fi,17a,21 trihydroxy 600,163 dimethyl-l,4-pregnadiene-3,20-dione, and its 21-acetate.

To a cooled solution of 436 mg. of 11fi,170t,2l-trihydroxy 60,1600 dimethyl 4 pregnene 3,20 dione 2l-acetate (which can be prepared as described hereinabove) in 2.5 cc. dimethyl formamide and 2.0 ml. of dry pyridine -is added 1.0 ml. of methane sulfonyl chloride, while maintaining the temperature below 0 C. The resulting mixture is allowed to warmlto room temperature, at whichpoint a precipitate appears; the resulting mixture is then heated to a temperature of about 70- 100 C. for a period of about 10 minutes. About 15 ml. of water is added slowly to the reaction mixture, with stirring, and the aqueous mixture is extracted with ethyl acetate. The combined ethyl acetate extracts are washed with water, then with dilute aqueous hydrochloric acid solution, again with water, and then with a dilute aqueous sodium bicarbonate solution. The washed ethyl acetate solution is dried, and the solvent is evaporated in vacuo; the residual material is triturated with ether, and the crystalline material is recrystallized to give 1711,21-dihYdlOXY- 60,160L dimethyl 4,9(11) pregnadiene 3,20-dione 2l-acetate. A suspension of 330 mg. of l70t,2l-dihydroxy- 60,1601 dimethyl 4,9(11) pregnadiene 3,20 L dione 2l-acetate and 1.8 g. of N-bromosuocinimide in a mixture of 50 ml. of diox-ane and 10 ml. of water is cooled to 10 C. Then with stirring, 10 ml. of cold 1.0 N aqueous perchloric acid is added. The temperature of the reaction mixture is allowed to rise to 15 C. and is maintained at this point for about two and one-half hours during which time the solid material slowly dissolves. The resulting yellow solution is treated with 1.0 ml. of allyl alcohol to discharge the color and the remaining N-bromo-succinimide, and the resulting solution is evaporated to a small volume in vacuo. The concentrated solution is diluted with water, and the aqueous mixture is extracted with ethyl acetate. The ethyl acetate extracts are :washed, dried and evaporated to dryness, and the residual material is crystallized from ethyl acetate-ether to give t-bromo-11fi, 1706,21 trihydroxy 601.,16Ct dimethyl 4 pregnene- 3,20-dione 21-acetate.

A solution of 210 mg. of 90t-bromo-11,8,17u,21-trihydroxy 601,160: dimethyl 4 pregnene 3,20 dione 21- acetate and 240 mg. of potassium acetate in 10 ml. of absolute ethanol is heated under reflux for two hours. The reaction mixture is cooled to room temperature, evaporated in vacuo to a small volume, and diluted with water. The concentrated aqueous mixture is extracted with three portions of ethyl acetate, and the combined ethyl acetate extracts are washed with water, dried, and evaporated to dryness in vacuo. The residual material is crys- 23 tallized from ethyl acetate-ether to give 9fl,l1fi-epoxy- 1704,21 dihydroxy 604,160: dimethyl 4 pregnene- 3,20-dione 21-acetate.

To a solution of 83 mg. of anhydrous hydrogen fiuoride in 4.7 ml. of ice-cold alcohol-free chloroform is added an ice-cold solution of 416 mg. of 95,11B-epoxy- 170;,21 dihydroxy 6a,l6a dimethyl 4 pregnene- 3,20-dione 21-acetate. The solution is mixed thoroughly and maintained at C. for two hours, at the end of which time 13.0 ml. of ice-cold 20% aqueous sodium acetate is added, and the resulting mixture agitated vigorously. The layers are separated, and the chloroform layer is washed with water until free of acid, dried, and the chloroform evaporated in vacuo. The residual material is crystallized from acetone-petroleum ether to give 90- fluoro l1B,17 x,21 trihydroxy 60;,16a dimethyl 4- pregnene-3,20-dione 21-acetate. Fifty milligrams of 90afluoro 11,B,17a,21 trihydroxy 6u,16ot dimethyl 4- pregnene-3,20-dione ZI-acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of 1 N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about 10 minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is purified by crystallization to give 9a-fluoro-11p,17u,21-trihydroxy- 6m,16a-dimethyl-3,20-dione.

Similarly, when hydrogen chloride is substituted for hydrogen fluoride in the reaction with 9B,11,B-epoxy-17u, 21 dihydroxy 6ot,16a dimethyl 4 pregnene 3,20- dione 21-acetate there is obtained the corresponding 90:- chloro l1B,17a,21 trihydroxy 60,l60t dimethyl 4- pregnene-3,20-dione.

In accordance with the foregoing procedures when 11ft, 17a,21 trihydroxy 60:,16/3 dimethyl 4 pregnene- 3,20-dione 21-acetate is employed as the starting material, there is obtained the corresponding 9ot-fiuoro-11p,17a,21- trihydroxy 6a,16;8 dimethyl 4 pregnene 3,20 dione or 9oz chloro 11,6,l7u,21 trihydroxy 6oz,16,B dimethyl-4-pregnene-3,20-dione.

To a solution of 100 mg. of 9ot-fluoro-11,8,17a,21-trihydroxy 6u,16a dimethyl 4 pregnene 3,20 dione 21-acetate, in 6 ml. t-butanol, and 0.01 ml. of glacial acetic acid is added 70 mg. of selenium dioxide. The mixture is heated under reflux in a nitrogen atmosphere for a period of about 60 hours. The reaction solution is filtered and evaporated in vacuo. The residual material is dissolved in benzene, and the benzene solution is washed with an aqueous sodium bicarbonate solution and dried over anhydrous sodium sulfate. The benzen solution is stirred with mercury overnight, then centrifuged, and the clear benzene solution is evaporated in vacuo. The residual material thus obtained is separated, using partition chromatography on diatomaceous silica (Super Cel), to give 9a-fluoro-11/8,17a,21-trihydroxy-6a,16ot-dimethyl-1,4-pregnadiene-3,ZO-dione 21-acetate.

This material is hydrolyzed using 1 N methanolic potassium hydroxide in benzene as described above for the hydrolysis of 90t-flL1OIO-11,5,1706,21-tl'lhYdIOXY-605,1606-(11- methyl-4-pregnene-3,20-dione 21-acetate to give 9u-fluoro- 1l}9,17a,21 trihydroxy 6(X,16OL dimethyl 1,4 pregnadiene-3,20-dione.

Starting with 9a-chloro-llfl,l7ot,2l-trihydroxy-6rx,l6adimethyl-4-pregnene-3,20-dione 2l-acetate, there are obtained in accordance with the foregoing procedures the corresponding 90: chloro-11,8,17ot,21-trihydroxy-6a,16adimethyl-l,4-pregnadiene-3,ZO-dione, and its 21-acetate.

Similarly, starting with 90c bromo l1fi,17oc,21 trihydroxy 6a,16a-dimethyl-4-pregnene-3,20-dione 21-acetate obtained as an intermediate in the preparation of 9afluoro-l1B,l7a,2l-trihydroxy-6oc,l6a-dimethyl 4 pregnene-3,20-dione herein described above, there are obtained the corresponding 90c bromo 11,8,17oc,21 t-rihydroxy-6a, 16a-dimethyl-1,4-pregnadiene-3,20-dione, and its ZI-acetate.

In accordance with the foregoing procedures, but starting with 9a-halo-1l5,l7a,21-trihydroxy-6a,l6u-dimethyl-4-pregnene-3,ZO-dione 2l-acetate there are obtained the corresponding 9a-holo-l1p,17ot,21-trihydroxy- 6a,16fl-dimethyl-1,4-pregnadiene-3,ZO-diones such as for example 9a-fiuoro-l1fi,17ot,2l trihydroxy-6a,l6B-dimethyl-l ,4-pregnadiene-3,20-dione, 9a chloro-1 1fl,17u,21-trihydroxy-6a,16fl-dimethyl-1,4-pregnadiene-3,ZO-dione and 9tx-bromo-11p,17a,21-trihydroxy-6ot,16B dimethyl 1,4- pregnadiene-3,20-dione, and their 21-acetates.

A solution of 400 mg. of 9ot-fluoro-llB,17a,2l-trihydroxy 6u,16a-d'imethyl-A-pregnene-3,20-dione 2l-acetate in 4 ml. of pyridine is added to the complex formed by the addition of 400 mg. of chromium trixode to a 4 ml. of pyridine. The mixture is swirled until thoroughly mixed and then allowed to stand at room temperature overnight. The reacton mixture is poured into water, and the aqueous mixture is extracted with ether and then twice with ethyl acetate. The combined ether and ethyl acetate extracts are washed with dilute aqueous sulfuric acid at about 0 C., and then with water until neutral. The organic solvent layer is then dried, the solvents are evaporated therefrom in vacuo, and the residual crystalline material is purified by crystallization to give 9a-fiuoro- 170t,21-CllhydfOXy-60t,160t-dll'll6thYl-4-Pl'6gl'l6l'l8 3,11,20- trione Zl-acetate. Fifty miligrams of 9a-fluoro-l7a,21-dihydroxy-6u,16u-dimethyl-4-pregnene 3,11,20 trione 21- acetate is dissolved in a mixture of 1.0 cc. of benzene and 1.0 cc. of l N methanolic potassium hydroxide, and the solution is allowed to stand at room temperature for a period of about 10 minutes. The solution is then acidified with acetic acid, the benzene is evaporated in vacuo, and the residual material is purified by crystallization to give 9a-fiuoro-l7rx,21-dihydroxy-6ot,16tx-dimethyl-4-pregnene-3,11,20-trione.

Similarly, starting with chloro ll{3,l7a,2l trihydroxy-60rd6ot-dimethyl-4-pregnene-3,20-dione 21-acetate, there are obtained in accordance with the foregoing procedures the corresponding 9a-chlorol7u,21-dihydroxy-6a, 16a-dimethyl-4-pregnene-3,11,20-trione, and its 21-acetate.

Similarly, but starting with 9a-bromo-11fi,17a,21-trihydroxy-6a,16a-dimethyl-4-pregnene-3,20-dione 21 -acetate obtained as an intermediate in the preparation of 9afluoro l1fl,l7o,2l trihydroxy-6a,l6zx-dimethyl-4-pregnene-3,20-dione herein described above, there are obtained the corresponding 9a-bromo-17a,21-dihydroxy-6a,l6ot-dimethyl-4-pregnene-3,l1,20-trione, and its 21-acetate.

In accordance with the foregoing procedures, but starting with 9a-halo-1lfi,l7a,21-trihydroxy-6a,16B-dimethyl- 4-pregnene-3,20-dione 21-acetate, there are obtained the corresponding 90c halo-l7a,2l-dihydroxy-orx,ldfl-dimethyl-4-pregnene-3,11,20-triones, such as for example, 90:- fiuoro 17a,2l-dihydroxy-6a,16B-dimethyL4-pregnene-3, 11,20-trione, 9a-chloro-l7u,2l-dihydroxy-6tx,16,8-dimethyl-4-pregnene-3,l1,20-trione, and 9a-bromo-l7rx,2l-dihydroxy 6a,l6,8 dimethyl-4-pregnene-3,11,20-trione, and their 2l-acetates.

To a solution of mg. of 9u-fiuoro-17a,'21-dihydroxy-6a,16u-dimethyl-4-pregnene-3,11,20-trione 2l-acetate, in 6 ml. t-butanol, and 0.01 ml. of glacial acetic acid is added 7 0 mg. of selenium dioxide. The mixture is heated under reflux in a nitrogen atmosphere for a period of about 60 hours. The reaction solution is filtered and evaporated in vacuo. The residual material is dissolved in benzene, and the benzene solution is washed with an aqueous sodium bicarbonate solution and dried over anhydrous solution sulfate. The benzene solution is stirred with mercury overnight, then centrifuged, and the clear benzene solution is evaporated in vacuo. Theresidual material thus obtained is separated using partition chromatography on diatomaceous silica (Super-Gel) to give 9afluoro 17a, 2l-dihydr-oxy-oa,l6ot-dimethyl-1,4-pregnadiene-3,11,20-trione 21 acetate. This material is hydrolyzed using 1 N .methanolic potassium hydroxide in benzene as described hereinabove for the hydrolysis of a fluoro 170:,21 dihydroxy-6a-dimethyl 4 pregnene-3,11,20-trione 21-acetate to give 90t-fillOI'O-170t,21dlhydroxy-6a,16u-dimethyl-1,4-pregnadiene-3,l1,20-trione.

Similarly, starting with 90t-ChlOIO-170z,21-dihydf0Xy-60c, 16u-dimethyl-4apregnene-3,11,20-trione 2l-acetate there are obtained in accordance with the foregoing procedures the corresponding 9wchloro-17a,21-dihydroxy-6a-dimethyl-1,4-pregnadiene-3,11,20-trione, and its 21-acetate.

Similarly, but starting with 9a-bromo-l7a,2l-dihydroxy-6a,16ot-dimethyl-4-pregnane-3,11,20-trione 21 acetate there are obtained the corresponding 9a-bromo-17ot, 2l-dihydroxy-6a,16a-dimethyl-1,4-pregnadiene 3,1l,20- trione, and its 21-acetate.

In accordance with the foregoing procedures but starting with 9a-halo-17a,21-dihydroxy-6a,16/i-dimethyl-4- pregnene-3,1r1,20-trione 2l-acetate there are obtained the corresponding 9a-halo-17a,21-dihydroxy-6 z,lofi-dimethyl- 1,4-pregnadienes-3,l'1,2 -triones, such as for example, 9afluoro 170:,21 dihydroxy-6ot,16B-d-imethyl-11,4-pregnadiene3,1 1,20-trione, 9ot-chloro-17u21-dihydroxy6a,16,B-dimethyl 'l,4pregnadiene-3,1 1,20-trione and 9a-bromo-17a, 21 dihydroxy 6a,16i-dimethyl-1,4-pregnadiene-3,l1,20= trione, and their Z1-acetates.

A suspension containing 300 mg. of 17a,21-dihydroxy- 6a,16u-dimethyl-4-pregnene-3,-1 1,2 0-trione 21-acetate and 1.7 ml. of acetic acid is refluxed for 17 hours under nitrogen. The reaction mixture is dil-uted with 40 ml. of ethyl acetate and filtered. The filtrate is washed sequentially with two 20 ml. portions of ice cold 10% aqueous sodium bisulfite solution, three 20 ml. portions of ice cold aqueous potassium hydroxide solution and finally washed to neutrality with several 20 ml. portions of ice Water. The aqueous washes are re-extracted with 50 ml. of ethyl acetate and treated as above. The combined organic phase is dried over sodium sulfate and concentrated in vacuo. The crude material dissolved in benzene is chromatographed on 15 g. of acid-Washed alumina. Elution With chloroformzether 2:8 affords 17a,21-dihydroxy-6,16a-dimethyl 4,6'pregnadiene-3,1 1,20-trione ZI-acetate. This product is then hydrolyzed by treatment with a solution of potassium bicarbonate in aqueous methanol to form 170:, 21 dihydroxy 6,160: dimethyl-4,6-pregnadiene-3,11,20- trione.

In accordance with the above procedure but starting With 170;,211 dihydroXy-6m,16B-dimethyl-4-pregnene-3, l1, 20-trione 2|1-acet-ate there are obtained l7u,2l-dihydroxy- 6,16fi-dimethyl-4,6-pregnadiene-3,11,20-trione and its 21- acetate.

In accordance with the above procedure but starting with 11B,17a,21 trihydroxy-6a,1 6oc-dimethyl-4-pregnene- 3,2 0-dione ZI-acetate there is obtained 11,B,17a,21-trihydroxy-6,16ot-dimethyl-4,6-pregnadiene-3,ZO-dione and its 21.-acetate.

In accordance with the above procedure but starting with ll 3,'l7u,21 trihydroxy-6u,16,6-dimethyl-4-pregnene- 3,20dione 2l-acetate there is obtained 1|1fl,17a,21-trihydroxy-6,16fi-dimethyl-4,6-pregnadiene-3,20-dione and its 21-acetate.

A suspension containing 300 mg. of 9u-fluoro-11/3,17u, 21 trihydroxy-M,16a-dimethyl-4-pregnene-3,ZO-dione 21- acetate, 70 0 mg. of chloranil, 8.3 ml. of ethyl acetate and 1.7 ml. of acetic acid is refluxed for 17 hours under nitrogen. The reaction mixture is diluted with 40 ml. of ethyl acetate and filtered. The filtrate is washed sequentially with two 20 ml. portions of ice cold aqueous sodium bisulfite solution, three 20 ml. portions of ice cold 5% aqueous potassium hydroxide solution and finally Washed to neutrality with several 20 ml. portions of ice Water. The aqueous washes are re-extracted with 50 ml. of ethyl acetate and treated as above. The combined organic phase is dried over sodium sulfate and concentrated in vacuo. The crude material dissolved in benzene is chromatographed on g. of acid-washed alumina. Elution with chloroformzether 2:8 affords 9a-fluoro-11fi-17a,21- trihydroxy-6,16a-dimethyl-4,6-pregnadiene-3,20-dione 21- acetate. This product is then hydrolyzed by treatment with a solution of potassium bicarbonate in aqueous methanol to form 9a-fiuoro-115,17a,21-trihydroxy-6,16a-d-imethylpregnadiene-lZO-dione.

In accordance with the above procedure but starting with 9a-ch1oro-1 1f ,17u,2l-trihydroxy-6a,l6a-dimethyl-4- pregnene-3,20-dione 21-acetate, there are obtained the corresponding 9oz chloro 1l5,17a,21-trihydroxy-6u,16a-dimethyl-4,6-pregnadiene-3,ZO-dione and its 21-acetate.

In accordance with the above procedure but starting with bromo-11,8,17a,21-trihydroXy-6,l6u-dimethyl-4- pregnene-3,20-dione ZI-acetate, there are obtained the corresponding 90: bromo llfi,l7oz,2l trihydroxy-6,16et-dimethyl-4,6-pregnadiene-3,2 0 dione and its 21-acetate.

Similarly, in accordance with the above procedure but starting with 9a-fiuoro-11/3,l7u,21-trihydroxy-6a,l6oz-dimethyl-4-pregnene-3,20-dione 21-acetate, there is obtained the corresponding 9a-fluoro-l 1 6, 1 7a:,2l-trihydroxy-6,16udimethyl-4,6-pregnadiene-3,ZO-dione and its 21-acetate.

Similarly, in accordance with the above procedure but starting with 9ot-ch1oro-11,8,17a,21-trihydroxy-6a,16;3-dimethyl-4-pregnene-3,20-dione ZI-acetate, there is obtained the corresponding 90t-ChlOTO-11,8,1711,21-tlilhYdl'OXY-6J6B- dimethyl-4,6-pregnadiene-3,2-0-dione and its 21-acetatc.

Similarly, in accordance with the above procedure but starting with 9a-bromo-1 1 3,17a,21-trihydroxy-6a,16B-dimethyl-4-pregnene-3,20-dione 2l-acetate, there is obtained the corresponding 9a-bromo-11fi,l7u,2l-trihydroxy-6,16ddimethyl-4,6-pregnadiene-3,ZO-dione and its 21-acetate.

A suspension containing 300 mg. of 9a-fiuoro-l7u,2ldihydroxy-6a,1 6a-dimethyl-4-pregnene-3,11,20-trione 21 acetate, 700 mg. of chloranil, 8.3 ml. of ethyl acetate and 1.7 ml. of acetic acid is refluxed for 17 hours under nitrogen. The reaction mixture is diluted with 40 m1. of ethyl acetate and filtered. The filtrate is Washed sequentially with two 20 ml. portions of ice cold 10% aqueous sodium bisulfite solution, three 20 ml. portions of ice cold 5% aqueous potassium hydroxide solution and finally Washed to neutrality with several 20 ml. portions of ice Water. The aqueous Washes are re-extracted with 50 ml. of ethyl acetate and treated as above. The combined organic phase is dried over sodium sulfate and concentarted in vacuo. The crude material dissolved in benzene is chromatographed on 15 g. of acid-Washed alumina. Elution With chloroformrether 2:8 affords 9u-fiuoro-17a,21-dihydroxy- 6,16a-dimethyl-4,6-pregnadiene3,l1,20-trione 2 1-acetate. This product is then hydrolized by treatment with a solution of potassium bicarbonate in aqueous methanol to form 9u-fiuoro-17a,21-dihydroxy-6,16ot-dimethyl-4,6-pregnadiene-3,11,20-trione.

In accordance with the above procedure but starting with 9a-ch1oro-17a,21-dihydroxy-6ot,16a-dimethyl-4-pregnene-3,11,20-trione 2l-acetate there is obtained the corresponding 9a-chloro-17a,21-dihydroxy-6,16a-dimethyl-4, 6-pregnadiene-3,11,20-trione and its 21-acetate.

In accordance with the above procedure, but starting with a 9tX-bI'OmO-170t,21-dlhydI'OXY 6ot,16a-dimethyl-4- pregnene-3,l1,20-trione 21-acetate there is obtained the corresponding 9a-bromo-17a,21-dihydroxy-6,16u-dimethyl-4,6-pregnadiene-3,11,20-trione and its 21-acetate.

Similarly, in accordance With the above procedure but starting with 9u-fluoro-17a,21-dihydroxy-6a,16a-dimethyl- 4-pregnene-3,11,20-trione 21-acetate, there are obtained the corresponding 9a-fluoro 17a,21-dihydr-oxy-6,16u-dimethyl-4,6-pregnadiene-3,11,20-trione and its ZI-acetate.

Similarly, in accordance with the above procedure but starting with 9a-fluoro-l7u,21-dihydroxy-6a,16,8-dimethyl- 4-pregnene-3,11,20-trione ZI-acetate, there are obtained the corresponding 9ot-fiuoro 17a,21-dihydroxy-6,16,8-dimethyl-4,6-pregnadiene3,1l,20-trione and its 21-acetate.

Similarly, in accordance with the above procedure but starting with 9ot-bromo-17ot,21-dihydr0xy-6a,16,8-dimethyl- 4-pregnene-3,11,20-trione 21-acetate, there are obtained the corresponding 9a-bromo-17a,21-dil1ydroxy-6,165-dimethyl-4,6-pregnadiene-3,11,20-trione and its 21-acetate.

To a solution of 200 mg. of 17u,21-dihydroxy-6,16rx-dimethyl4,6-pregnadiene-3,11,20-trione 21-acetate in 0.16 ml. of acetic acid and 12 ml. of t-amyl alcohol is added 120 mg. of selenium dioxide and 2 drops of mercury. The mixture is refluxed under nitrogen overnight. The solution is filtered, washed with sodium bicarbonate, dried, and concentrated. This product is chromatographed on acid washed alumina. The adsorbate is eluted with mixtures of chloroform and ether, increasingly rich in cholorform. The eluates are combined, evaporated to dryness and the residual material recrystallized from ethyl acetate to give 17a,21-dihydroxy 6,16a-dimethyl 1,4,6-pregnatriene'3, 11,20-trione 21-acetate. This product is then hydrolyzed by treatment with a solution of potassium bicarbonate in aqueous methanol to form 17a,21-dihydroxy 6,16u-Cllmethyl-1,4, 6-pregnatriene-3 ,1 1,20-trione.

In accordance with the above procedure but starting with 17:1,21-ClihYdIOXY 6,165-1dimethyl-4,6-pregnadiene- 3,11,20-trione 21-acetate there are obtained 17a,21-dihydroxy-6,165-dimethyl 1,4,6-pregnatriene-3,11,20-trione and its 21-acet-ate.

Similarly, when 1l5,17or,21-trihydroxy-6,16oc-dimethyl- 4,6-pregnadiene-3,20-dione 21-acetate is used as starting material in the foregoing reaction with selenium dioxide and the pro-duct hydrolyzed with aqueous methanolic potassium bicarbonate solution, there are obtained 115,170, 21-trihydroxy-6,16u-dimethyl 1,4,6-pregnatriene-3,20-dione and its 21-acetate. Where the starting material in this procedure is 115,17a,21-trihydrxy 6,165-dimethyl-4,6- pregnadiene-3,20-dione 21-acetate, there are obtained 1 15,17a,21-trihydr-oxy-6,165-dimethyl 1,4,6-pregnatriene- 3,20-dione and its 21-acetate.

Where the starting material in the foregoing reaction with selenium dioxide followed by hydrolysis with aqueous methanolic potassium bicarbonate is 9ozfil10rO-11}3,17oc,2ltrihydroxy-6,16a-dimethyl-4,6-pregnadiene-3,30-dione 21- acetate, the products obtained are 9u-fi11OIO-l1,8,17or,21- trihydroxy-6,16rx-dimethyl 1,4,6-pregnatriene-3,20-dione and its 21-acetate.

In accordance with the above procedure but starting with 9a-chloro-115,17a,21-trihydroxy-6,16a-dimethyl-4,6- pregnadiene-3,20-dione 21-acetate there are obtained 90:- chloro 115,17a,21 trihydroxy 6,16a dimethyl-1,4,6- pregnadiene-3,20dione and its 21-acetate.

Similarly, in accordance with the above procedure but starting with 9u-bromo-115,17a,21-trihydroxy-6,16a-dimethyl-4,6-pregnadiene-3,ZO-dione 21 acetate there are obtained 9or-b1'OII10-1 15,17a,21-trihydroxy-6,16a-dimethyl- 1,4,6-pregnatriene-3,20-dione and its 21-acetate.

In accordance with the above procedure but starting with 9ot-fiuoro-115,17a,21-trihydroxy-6,165-dimethyl-4,6- pregnadiene-3,20-dione 21-acetate there are obtained 90:- fluoro 11,/3,170c,21 trihydroxy 6,165 dimethyl 1,4,6- pregnatriene-3,20-dione and its 21-acetate.

In accordance with the above procedure but starting with 9or-chloro-115,17u,21-trihydroxy 6,165 dimethyl- 4,6-pregnadiene-3,20-dione 21-acetate there are obtained 90c chloro l15,l7oc,21 trihydroxy 6,165 dimethyl- 1,4,6-pregnatriene-3,20-dione and its 21-acetate.

In accordance with the above procedure but starting with 9or-bromo-115,17a,21-trihydroxy-6,165-dimethyl-4,6- pregnadiene-3,20-dione 21-acetate there are obtained 90:- bromo 115,17a,21 trihydroxy 6,165 dimethyl-1,4,6 pregnatriene-Ii,20-dione and its 21-acetate.

To a solution of 200 mg. of 9u-fluoro-17a,21-dihydroxy- 6,16a-dimethyl-4,6-pregnadiene-3,11,20-trione 21 acetate in 0.16 ml. of acetic acid and 12 ml. of t-amyl alcohol is added 120 mg. of selenium dioxide and 2 drops of mercury. The mixture is refluxed under nitrogen overnight. The solution is filtered, washed with soduim bicarbonate, dried, and concentrated. This product is chromatographed on acid-washed alumina. The adsorbate is eluted with mixtures of chloroform and ether, increasingly rich in chloroform. The eluates are combined, evaporated to dryness and the residual material recrystallized from ethyl acetate to give 9or-fiuoro-17a,21-dihydroxy-6,16a-dimethyl-1,4,6-pregnatriene-3,11,20-trione 21-acetate. This product is then hydrolyzed by treatment with a solution of potassium bicarbonate in aqueous methanol to form fluoro 1701,21 dihydroxy 6,160: dimethyl 1,4,6- pregnatriene-3,11,20-trione.

In accordance with the above procedure but starting with 9a-chloro-17u,21-dihydroxy-6,16a-dimethyl-4,6-pregnadiene-3,11,20-trione 21-acetate there are obtained 9achloro 1704,21 dihydroxy 6,16a dimethyl 1,4,6- pregnatriene-3,11,20-trione and its 21-acetate.

Similarly, in accordance with the above procedure but starting with 9a-bromo-17u,21-dihydr0xy-6,16u-dimethyl- 4,6-pregnadiene-3,11,20-trione 21-acetate there are obtained 9a-bromo-17oc,21dihydroxy-6,16a-dimethyl-1,4,6 pregnatriene-S,l1,20-trione and its 21-acetate.

In accordance with the above procedure but starting with 9or-fluoro-17a,21-dihydroxy-6,165-dimethyl-4,6-pregnadiene-3,11,20-trione 21-acetate there are obtained 9afluoro 1711,21 dihydroxy 6,165 dimethyl 1,4,6- pregnatriene-3,11,20-trione and its 21-acetate.

In accordance with the above procedure but starting with 9a-chloro-l7a,21-dihydroxy-6,l65-dimethyl-4,6-pregnadiene-3,11,20-trione 21-acetate there are obtained 9achloro 17oc,21 dihydroxy -6,l65 dimethyl 1,4,6- pregnatriene-3,11,20-trione and its 21-acetate.

In accordance with the above procedure but starting with 9er-bromo-17a,21-dihydroxy-6,165-dimethyl-4,6-pregnadiene-3,11,20-trione 21-acetate there are obtained 90:- .bromo 17a,21 dihydroxy 6,165 dimethyl 1,4,6- pregnatriene-3,11,20-trione and its 21-acetate.

To a suspension of 25.0 g. of 115,17a,21-trihydroxy- 6,16a-dimethyl-4,6-pregnadiene-3,20-dione in 1.5 l. of alcohol-free chloroform cooled to about 5 C. in an ice bath is added with constant stirring 750 ml. of cold, concentrated aqueous hydrochloric acid solution and then 750 ml. of formalin (low in methanol). The mixture is removed from the ice bath and stirred at room temperature for approximately 7 hours. The layers are separated and the aqueous phase is back-extracted twice with chloroform. The combined chloroform layers are washed twice with a 5% aqueous solution of sodium bicarbonate, and twice with a saturated aqueous solution of sodium chloride. The washed chloroform solution is dried over magnesium sulfate and evaporated under reduced pressure. The residual material is triturated with methanol to give a crystalline solid, which is recrystallized from a mixture of benzene and n-hexane to give 17a,2(),20,21-bismethylenedioxy-l 15, hydroxy-6,16a-dirnethyl-4,6-pregnadiene-3- one.

A solution of 400 mg. of 17a,20,20,2l-bismethylenedioxy--hydroxy-6,16a-dimethyl-4,6-pregnadiene-3-one in 4 ml. of pyridine is added to the complex formed by the addition of 400 mg. of chromium trioxide to 4 ml. of pyridine. The mixture is swirled until thoroughly mixed and then allowed to stand at room temperature fora period of about 15 hours. The reaction mixture is poured into water, and the aqueous mixture is extracted with ether and then twice with ethyl acetate. The combined ether and ethyl acetate extracts are washed with dilute aqueous sulfuric acid at about 0 C., and then with water until neutral. The organic solvent layer is then dried, the solvents are evaporated therefrom in vacuo, and the residual crystalline material is purified by crystallization from a mixture of ethyl acetate and ether to give 17a,20,- 20,21-bismethylenedioxy-6,16a-dimethyl-4,6-pregnadiene- 3,11-dione.

Approximately 1.35 g. of 17a,20,20,2l-bismethylenedioxy 6,16a dimethyl 4,6 pregnadiene 3,11 dione is dissolved in 23 ml. of dry, hot benzene, the resulting solution is cooled to room temperature, and to the solution is added 0.96 ml. of freshly-distilled ethyl formate. The air in the system is replaced with nitrogen and 560 mg. of sodium hydride (as a 58% dispersion in mineral oil) is added. The system is again evacuated and filled with nitrogen, and the mixture is stirred at room temperature for a period of about 15 hours. The reaction mixture is poured into an excess of a saturated aqueous solution of sodium dihydrogen phosphate, and the resulting aqueous mixture is extracted four times with benzene. The benzene reaction solution and extracts are combined, washed three times with water, dried over sodium sulfate, and evaporated to dryness. The residual material is dissolved in ether, and the ether solution is extracted with a 10% aqueous solution of sodium carbonate. The aqueous alkaline extracts are acidified with an excess of a saturated aqueous solution of sodium dihydrogen phosphate, and the aqueous acidic mixture extracted with ether and then with chloroform. The combined organic extracts are dried over sodium sulfate, and evaporated to dryness to give 1704,2020,- 21 bismethylenedioxy 2 hydroxy methylene 6,160:- dimethyl-4,6-pregnadiene-3,1l-dione.

Approximately 850 mg. of 17u,20,20,2l-bismethylenedioxy 2 hydroxymethylene 6,16u dimethyl 4,6- pregnadiene-3,11-dione is dissolved in 9.2 ml. of absolute ethanol, and to the solution is added a solution of 0.16 ml. of hydrazine hydrate dissolved in 0.16 ml. of absolute ethanol. The resulting mixture is heated under reflux in a nitrogen atmosphere for a period of about 45 minutes, and the reaction mixture is then evaporated to dryness under reduced pressure. The residual material is washed with three portions of cold water, and the resulting amorphous solid is dried at a temperature of about 80 C. for 1 hour in high vacuum to give 17a,20,20,2l-bismethylenedioxy 6,1611 dimethyl [3,2 c]pyrazolo 4,6 pregnadiene-l l-one.

To a solution of 100 mg. of 17a,20,20,21-bismethylenedioxy 6,160; dimethyl [3,2 clpyrazolo 4,6 pregnadiene-l l-one in 2 ml. of pyridine is added 0.5 ml. of acetic anhydride. The mixture is allowed to stand overnight at room temperature. A mixture of ice and water is then added. After standing for about 30 minutes, the product is extracted with e tliyl acetate. The ethyl acetate extract is washed successively'with water, with ice-cold 1 N sulfuric acid (until thepH of the aqueous layer is 1-3), with saturated aqueous sodium bicarbonate solution (until the pH of theaqueous layer is '8), and with Water (until the aqueous layer is neutral). The ethyl acetate solution is then dried with anhydrous sodium sulfate, and the solvent is distilled at a temperature of about 40 C., in'vacuo to give 1 acetyl 17d,Z0,20,21 bismethylenedioxy 6,160:- dimethyl [3,2 c]pyrazolo- 4,6 pregnadiene 11 one, which is isolated by the addition of water and filtration.

In accordance with the above procedure, but using an equivalent quantity of another acylating agent in place of the acetic anhydride, there is obtained the corresponding 1-acyl derivative.

Approximately 72 mg. of 1'-acetyl-l7a,20,20,2l-bismethylenedioxy 6,160: dimethyl [3,2 cJpyrazolo- 4,6-pregnadiene-l l-one is heated on a steam bath with 24 ml. of a 60% aqueous solution of formic acid for a period of about 30 minutes. The excess reagent is removed in vacuo using a water bath at a temperature of about 50 C. as the source of heat. The residual material is flushed four times with n-hex-ane, and dried at 60 C. in high vacuum. The amorphous solid thus obtained is dissolved in about 3.4 ml. of pure methanol and allowed to react with 1.3 ml. of a 1.33 N solution of sodium methoxide in methanol at room temperature under a nitrogen atmosphere for ten minutes. The excess sodium methoxide is neutralized with acetic acid, and the mixture is then evaporated to dryness and flushed with n-hexane. The residual material is washed with water, filtered and dried to give 17u,21-dihydroxy- 6,160; dimethyl-[3,2 c]pyrazolo 4,6 pregnadiene 11, ZO-dione.

In accordance with the above procedures, but starting with the 1lfi,l7a,2l-trihydroxy-6,l6fl-dimethyl-4,6-pregnadiene-3,20-dione in place of the llfi,17a,21trihydroxy- 6,1611 dimethyl 4,6 pregnadiene 3,20 dione, there is obtained as product the corresponding 17a,21-dihydroxy 6,16fl dimethyl [3,2 c]pyrazolo 4,6 pregnadiene-11,20-dione.

In accordance with the above procedures, but starting With l1fi,17a,21 trihydroxy 6,16oc dimethyl 9afluoro-4,6-pregnadiene-3,20-dione in place of the 1lfi,l7a,- 21 trihydroxy 6,16a dimethyl 4,6 pregnadiene- 3,20-dione, there is obtained as product, via the inter mediate formation of 1-acetyl-l7a,20,20,2l-bismethylenedioxy 6,160; dimethyl 9d fiuoro [3,2 c] pyrazolo- 4,6-pregnadiene-1l-one, the corresponding 17a,21-dihydroxy 6,16a dimethyl 9a fluoro [3,2 cJpyrazolo- 4,6-pregandiene-l1,20-dione. Alternatively, the intermediate 1 acetyl 17a,20,20,2l bismethylenedioxy- 6,16a dimethyl c fluoro [3,2 c]pyrazolo 4,6- pregnadiene-ll-one is reacted with sodium borohydride to form 1' acetyl 17a,20,20,21 bismethylenedioxy 6,16ocdimethyl 9oz fluoro [3,2 cJpyrazolo 4,6 pregnadiene-llfl-ol which is then reacted with 60% aqueous formic acid and the resulting amorphous solid reacted with dilute methanolic sodium methoxide as described hereinabove in this example, thereby forming 11,8,17u,21- trihydroxy 6,16ot dimethyl 90a fluoro [3,2 c] pyrazolo-4,6-pregnadiene-20-one.

Approximately 1.35 g. of 17a,20,20,2l-bismethylenedioxy-l1,6-hydroxy-6,16a-dimethyl 4,6 pregnadiene-3- one (which can be prepared as described hereinabove in this example) is dissolved in 23 ml. of dry, hot benzene, the resulting solution is cooled to room temperature, and to the solution is added 0.96 ml. of freshly-distilled ethyl formate. The air in the system is replaced with nitrogen and 560 mg. of sodium hydride (as a 58% dispersion in mineral oil) is added. The system is again evacuated and filled with nitrogen, and the mixture is stirred at room temperature for a period of about 15 hours. The mixture is poured into an excess of a saturated aqueous solution of sodium dihydrogen phosphate, and the resulting aque ous mixture is extracted four times: with benzene. The benzene reaction solution and extracts are combined, washed three times with water, dried over sodium sulfate, and evaporated to dryness. The residual material is dissolved in ether, and the other solution is extracted with a 10% aqueous solution of sodium carbonate. The aqueous alkaline extracts are acidified with an excess of a saturated aqueous solution of sodium dihydrogen phosphate, and the aqueous acidic mixture extracted with ether and then with chloroform. The combined organic extracts aredried over sodium sulfate, and evaporated to dryness to give 17a,20,20,2l-bismethylenedioxy-IIB-hydroxy-Z- hydroxymethylene-G,16a-dimethyl-4,6-pregnadiene-3-one.

Approximately 850 mg. of l7a20,20,21-bismethylenedioxy-l Lit-hydroxy 2 hydroxymethylene-6,l6a-dimethyl-4,6-pregnadiene-3one is dissolved in 9.2 ml. of absolute ethanol, and to the solution is added a solution of 0.16 ml. of hydrazine hydrate dissolved in 0.16 ml. of absolute ethanol. The resulting mixture is heated under reflux in a nitrogen atmosphere for a period of about 45 minutes, and the reaction mixture is then evaporated to dryness under reduced pressure. The residual material is washed with three portions of cold water, and the resulting amorphous solid is dried at a temperature of about 80 C. for 1 hour in high vacuum to give 17a,20,20,21- bismethylenedioxy 6,16a-dimethyl-[3,2-c]pyrazolo-4,6- pregnadiene-l 15-01.

To a solution of mg. of 17a,20,20,21-bismethylenedioxy-6,16a-dimethyl-[3,2-c]pyrazolo 4,6 pregnadiene-llB-ol in 2 ml. of pyridine is added 0.5 ml. of acetic anhydride. The mixture is allowed to stand overnight at room temperature. A mixture of ice and water is then added. After standing for about 30 minutes, the

product is extracted with ethyl acetate. The ethyl acetate extract is washed successively with water, with ice-cold 1 N sulfuric acid (until the pH of the aqueous layer is 1-3), with saturated aqueous sodium bicarbonate solution (until the pH of the aqueous layer is 8), and with water (until the aqueous layer is neutral). The ethyl acetate solution is then dried with anhydrous sodium sulfate, and the solvent is distilled at a temperature of about 40 C. in vacuo to give 1'-acetyl-17a,20,20,2l-bismethylenedioxy-6-l6a-dimethyl-[3,2-c]pyrazolo 4,6 pregnadiene-llfi-ol which is isolated by the addition of water and filtration.

In accordance with the above procedure, but using an equivalent quantity of another acylating agent in place of acetic anhydride there is obtained the corresponding 1-acyl-steroid.

Approximately 720 mg. of l'-acetyl-17u,20,20,2l-bismethylenedioxy 6,16 dimethyl [3,2-c]pyrazolo-4,6- pregnadiene-llfl-ol is heated on a steam bath with 24 ml. of a 60% aqueous solution of formic acid for a period of about 30 minutes. The excess reagent is removed in vacuo using a water bath at a temperature of about 50 C. as the source of heat. The residual material is flushed four times with n-hexane, and dried at 60 C. in high vacuum. The amorphous solid thus obtained is dissolved in about 3.4 ml. of pure methanol and allowed to react with 1.3 ml. of a 1.33 N solution of sodium methoxide in methanol at room temperature under a nitrogen atmosphere for ten minutes. The excess sodium methoxide is neutralized with acetic acid, and the mixture is then evaporated to dryness and flushed with n-hexane. The residual material is washed with water, filtered and dried to give l1fi,l7a,2l trihydroxy 6,16ot-dimethyl-[3,2-c] pyrazolo-4,6-pregnadiene-20-one.

Approximately 0.5 g. of 17a,20,20,2l-bismethylenedioxy-1lfl-hydroxy-6,16ot-dimethyl 4,6 pregnadiene-3- one is dissolved in 25 cc. of benzene, and about 5 cc. of benzene is removed from the solution by distillation at normal pressure The resulting solution is cooled to room temperature, and to the solution is added about 0.75 cc. of freshly-distilled ethyl formate. The air in the system is replaced with nitrogen, and about 150 mg. of sodium hydride (as a 57% dispersion in mineral oil) is added. The mixture is stirred under nitrogen at room temperature for a period of about three hours. About cc. of a saturated aqueous solution sodium dihydrogen phosphate is added to the reaction mixture and the re- ;sulting aqueous mixture is extracted with ether. The benizene solution and ether extracts are combined, extracted with 2 N aqueous sodium hydroxide, and the aqueous :sodium hydroxide extracts are acidified with sodium dihydrogen phosphate. The aqueous acidified solution is extracted with ether, the ether extract is evaporated to dryness, and the residual material is crystallized from ether to give 17a,20,20,2l-bisrnethylenedioxy-llfi-formyloxy 2 hydroxymethylene-6,l6u-dimethyl-4,6-pregnadiene-3-one. Evaporation of the ether mother liquor, followed by recrystallization of the residual material from ether gives substantially pure 171x,20,20,2l-bismethylenedioxy 11p hydroxy 2 hydroxyrnethylene-6,16ot-dimethyl-4,6-pregnadiene-3-one; M.P. ZOO-204 C.

Approximately 1.19 g. of l7ot,20,20,2l-bismethylenedioxy-1 1fi-hydroxy-Z-hydroxymethylene-6,16a dimethyl- 4,6-pregnadiene-3-one is dissolved in cc. of ethanol. Three hundred mg. of phenyl hydrazine is added, and the mixture is heated under reflux in a nitrogen atmosphere for one hour. About 25 cc. of water is added. The product is then extracted into 150 cc. of ether. The ether extracts are Washed with 2 N aqueous HCl, with saturated sodium bicarbonate, with water, with saturated aqueous sodium chloride solution, and then dried over anhydrous sodium sulfate. The washed and dried ether extracts are evaporated to dryness and the residual material is crystallized from other to give 17a,20,20,21-bisrnethyl- 32,. enedioxy-6,l6a-dimethyl-2-phenyl-[3,2-c]pyrazolo 4,6- pregnadiene-llfi-ol; M.P. 258-262 C.

Approximately 430 mg. of l7a,20,20,2l-bismethylenedioxy 6,160: dimethyl-2'-phenyl-[3,2-'c]pyrazolo-4,6- pregnadiene-llB-ol is heated on a steam bath under nitrogen with 40 cc. of a 60% aqueous solution of formic acid for a period of about 30 minutes. About 40 cc. of water is added to the reaction mixture, and the mixture is then extracted into about 200 cc. of chloroform. The chloroform solution is washed with Water, with saturated aqueous sodium bicarbonate solution, again with water, and is then dried over anhydrous sodium sulfate. The washed and dried chloroform solution is evaporated under vacuum and the residual product is dissolved in 60 cc. of absolute methanol, and 0.1 equivalent of sodium methoxide in methanol is added. The resulting mixture is stirred under nitrogen at room temperature for 15 minutes. The reaction mixture is acidified with acetic acid, and the solvent is evaporated under vacuum at room temperature. About 20 cc. of water is added to the residual material, and the aqueous mixture is extracted with about 150 cc. of ethyl acetate. The ethyl acetate solution is washed with saturated aqueous sodium bicarbonate solution, with water, and is then dried over anhydrous sodium sulfate and evaporated to dryness to give an amorphous solid. This amorphous solid is dried in a high vacuum, and is then dissolved in 4 cc. of pyridine. About 3 cc. of acetic 'anhydride is added. The resulting mixture is heated on the steam bath for about 15 minutes and evaporated to dryness in vacuo. About 20 cc. of water is added. The aqueous mixture is then extracted with about 150 cc. of ethyl acetate, the ethyl acetate extract is Washed with saturated aqueous sodium bicarbonate solution, and with water; and is then dried over anhydrous sodium sulfate. The washed and dried ethyl acetate solution is evaporated in vacuo, and the residual material is crystallized 'from ethyl acetate benzene to give substantially pure 11/3,17a,21-trihydroxy-6,16a-dimethyl- 2-phenyl- [3 ,2-c] pyrazolo-4,6pregnadiene-20-one 21-acetate; M.P. 225226 C.

One hundred mg. of 11B,17a,21-trihydroxy-6,16a-d-imethyl-2-phenyl-[3,2-c]pyraz0lo 4,6 pregnadiene-ZO- one 21-acetate is dissolved in 10 cc. of absolute methanol, and 1.1 equivalents of sodium methoxide in methanol is added. The mixture is stirred at room temperature under nitrogen for 15 minutes. The product is acidified with acetic acid and is then evaporated at room temperature under vacuum. The residual material is dissolved in cc. of chloroform, the chlorofrorn solution is washed with water, with saturated aqueous sodium bicarbonate solution, again with water, and is then dried over anhydrous sodium sulfate. The washed and dried chloroform solution is evaporated to dryness to give 115,170, 21-trihydroxy 6,160: dimethyl-2'-phenyl-[3,2-c1pyrazolo-4,6-pregnadiene20-one.

The 16-mono-N-acetylamido-2-deoxy-glucosides and galactosides of this invention are prepared from the corresponding 16-hydroxy-21-acylates such as the 21-acetate. The monoacetate is prepared as follows: a mixture of the 16,2l-diacetate and the 21-monoacetate prepared by treating the steroid substrate, for example, 9oc-fluOrO-11B,16cz, 17a,21-tetrahydroxy-1,4-pregnadiene-3,20-dione with 1.1 to 1.2 molar equivalents of acetic anhydride in pyridine is extracted with an excess of 0.1 M aqueous sodium tetraborate. The diacetate is insoluble. The 2l-monoacetate dissolves in the alkaline solution and precipitates on standing at room temperature after adjusting the pH to 1.2-2.0 with concentrated hydrochloric acid.

What is claimed is:

1. 115,17a dihydroxy 3,20 dione 1,4 pregnadiene 21 yl tri O acetyl p D 2 acetamido- 2-deoxy-glucoside.

2. 16a methyl llB,17oc dihydroxy 3,20 dione- 1,4 pregnadiene 21 yl tri O acetyl [3 D 2'- acetamido-2'-deoxy-glucoside. 

1. 11B,17A - DIHYDROXY - 3,20 - DIONE - 1,4 - PREGNADIENE - 21 - YL - TRI - 0 - ACETYL - B - D - 2'' - ACETAMIDO2''-DEOXY-GLUCOSIDE. 